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Dyspepsia in Pregnancy

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21. Lactoferrin Versus Ferrous Sulfate in Iron-deficiency During Pregnancy

Ferrous Sulfate in Iron-deficiency During Pregnancy Actual Study Start Date : January 15, 2018 Actual Primary Completion Date : October 30, 2018 Actual Study Completion Date : November 20, 2018 Resource links provided by the National Library of Medicine related topics: available for: Arms and Interventions Go to Arm Intervention/treatment Active Comparator: Lactoferrin Group Includes 49 pregnant women receiving lactoferrin 100 mg one sachet twice daily for 30 days to be dissolved in 1/4 glass of water (...) Lactoferrin Versus Ferrous Sulfate in Iron-deficiency During Pregnancy Lactoferrin Versus Ferrous Sulfate in Iron-deficiency During Pregnancy - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Lactoferrin

2018 Clinical Trials

22. Dyspepsia in Pregnancy

Dyspepsia in Pregnancy Dyspepsia in Pregnancy Toggle navigation Brain Head & Neck Chest Endocrine Abdomen Musculoskeletal Skin Infectious Disease Hematology & Oncology Cohorts Diagnostics Emergency Findings Procedures Prevention & Management Pharmacy Resuscitation Trauma Emergency Procedures Ultrasound Cardiovascular Emergencies Lung Emergencies Infectious Disease Pediatrics Neurologic Emergencies Skin Exposure Miscellaneous Abuse Cancer Administration 4 Dyspepsia in Pregnancy Dyspepsia (...) in Pregnancy Aka: Dyspepsia in Pregnancy , Gastroesophageal Reflux in Pregnancy , GERD in Pregnancy II. Evaluation Avoid diagnostic testing in pregnancy III. Management: First Line Agents ral Measures See See Drink 8 glasses (8 ounces) non-caffeinated fluid daily Decrease provocative foods Decrease or eliminate , chocolate, spicy foods Avoid milk products toward end of day Avoid fatty foods No eating food 2-3 hours before bedtime Elevate head of bed to 30 degrees First: s (may interfere with iron

2015 FP Notebook

23. Itch in pregnancy

in 5 pregnant women. Obstetric cholestasis is the main cause of itch without a rash in pregnancy. The itch (often severe) usually starts abruptly in the third trimester on the soles of the feet and palms of the hands, and spreads to become more generalized. It is often worse at night. Obstetric cholestasis generally poses no risk to the pregnant woman. Although it is associated with an increased risk of stillbirth, this appears to be only slightly raised above background rates with specialist (...) of itch associated with rash (including pregnant-specific dermatoses such as polymorphic eruption of pregnancy, atopic eruption of pregnancy, and pemphigoid gestationis). Scenario: Itch without rash Scenario: Management of itch in pregnancy without rash From age 13 years onwards (Female). Management of obstetric cholestasis How should I manage a woman with suspected obstetric cholestasis? Arrange admission to hospital, or same-day obstetrics referral for any woman with suggesting obstetric cholestasis

2015 NICE Clinical Knowledge Summaries

24. A Study to Evaluate the Effects of ABX-1431 on Patients With Functional Dyspepsia

A Study to Evaluate the Effects of ABX-1431 on Patients With Functional Dyspepsia A Study to Evaluate the Effects of ABX-1431 on Patients With Functional Dyspepsia - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding (...) more. A Study to Evaluate the Effects of ABX-1431 on Patients With Functional Dyspepsia The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT02875678 Recruitment Status : Terminated (recruitment challenges) First Posted : August 23, 2016 Last Update Posted : September 7, 2017 Sponsor: Abide Therapeutics

2016 Clinical Trials

25. Endoscopic Tri-Modal Imaging to Distinguish Functional Dyspepsia From Reflux Disease

Adult) Sexes Eligible for Study: All Accepts Healthy Volunteers: Yes Criteria Inclusion Criteria: symptoms suggestive of GERD or dyspepsia. Presence of symptom for longer than 6 month Provision of written informed consent Exclusion Criteria: Any known upper GI disease, other than reflux esophagitis Active or healing gastroduodenal ulcer (except scars) History of esophageal or gastric surgery. Clinically significant heart, lung, liver or kidney disease Allergy to proton-pump inhibitor Pregnancy (...) Endoscopic Tri-Modal Imaging to Distinguish Functional Dyspepsia From Reflux Disease Endoscopic Tri-Modal Imaging to Distinguish Functional Dyspepsia From Reflux Disease - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before

2016 Clinical Trials

26. Efficacy and Safety of Two Simeticone Brands in Adults With Functional Dyspepsia

the gastrointestinal tract and at least 7 days wash-out period. Females of childbearing potential must have a negative urine pregnancy test at the baseline visit. Male or non-pregnant, non-lactating female agree to the contraceptive requirements (including female partner's use of a highly effective form of birth control for at least 3 months before the study, during the study and for 3 months after the last dose of study drug) as outlined in Section 10.7.4. Able to read and understand the local language; Provide (...) Efficacy and Safety of Two Simeticone Brands in Adults With Functional Dyspepsia Efficacy and Safety of Two Simeticone Brands in Adults With Functional Dyspepsia - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding

2016 Clinical Trials

27. Therapeutic Effect of Ursodeoxycholic Acid in Functional Dyspepsia

Therapeutic Effect of Ursodeoxycholic Acid in Functional Dyspepsia Therapeutic Effect of Ursodeoxycholic Acid in Functional Dyspepsia - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Therapeutic Effect (...) of Ursodeoxycholic Acid in Functional Dyspepsia The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT03004118 Recruitment Status : Unknown Verified November 2016 by Universitaire Ziekenhuizen Leuven. Recruitment status was: Not yet recruiting First Posted : December 28, 2016 Last Update Posted : December 28, 2016

2016 Clinical Trials

28. Study to Evaluate Dietary Modification in Patients With Functional Dyspepsia.

Study to Evaluate Dietary Modification in Patients With Functional Dyspepsia. Study to Evaluate Dietary Modification in Patients With Functional Dyspepsia. - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more (...) . Study to Evaluate Dietary Modification in Patients With Functional Dyspepsia. The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT02863822 Recruitment Status : Withdrawn (no patients enrolled) First Posted : August 11, 2016 Last Update Posted : April 17, 2018 Sponsor: Advocate Health Care Information

2016 Clinical Trials

29. Clinical Trial to Assess the Efficacy and Safety of Combination Therapy of Motireb 5/100 mg in Functional Dyspepsia Patients.

Clinical Trial to Assess the Efficacy and Safety of Combination Therapy of Motireb 5/100 mg in Functional Dyspepsia Patients. Clinical Trial to Assess the Efficacy and Safety of Combination Therapy of Motireb 5/100 mg in Functional Dyspepsia Patients. - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached (...) the maximum number of saved studies (100). Please remove one or more studies before adding more. Clinical Trial to Assess the Efficacy and Safety of Combination Therapy of Motireb 5/100 mg in Functional Dyspepsia Patients. The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT02831543 Recruitment Status

2016 Clinical Trials

30. Feasibility and Acceptability of Maternal Choline Supplementation in Heavy Drinking Pregnant Women: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial. Full Text available with Trip Pro

Feasibility and Acceptability of Maternal Choline Supplementation in Heavy Drinking Pregnant Women: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial. Choline, an essential nutrient, serves as a methyl-group donor for DNA methylation and is a constituent of the neurotransmitter acetylcholine and a precursor to major components of cell membranes. Findings from animal studies suggest that choline supplementation during pregnancy can mitigate adverse effects of prenatal alcohol (...) ascertained using a timeline follow-back interview. By 4 weeks, plasma choline concentrations were significantly higher in the choline supplementation than the placebo arm, and this group difference continued to be evident at 12 weeks. The only side effect was a small increase in nausea/dyspepsia. No effects were seen for diarrhea, vomiting, muscle stiffness, blood pressure, or body odor changes.This study demonstrated that a choline supplementation program with very heavy drinkers during pregnancy

2018 Alcoholism, clinical and experimental research Controlled trial quality: predicted high

31. Management of Rapunzel Syndrome in a Four-month Pregnant Female with Twins: The First Reported Case? Full Text available with Trip Pro

Management of Rapunzel Syndrome in a Four-month Pregnant Female with Twins: The First Reported Case? A bezoar is a collection of packed indigestible matter that accumulates in the gastrointestinal tract after ingestion by the patient. It may be made of hair (trichobezoar), vegetable or fruit (phytobezoar), or other indigestible materials. Trichobezoars are thought to form due to hair's natural enduring nature, as they get matted and stick together in the gut. We present the case of a young (...) female who was 16-weeks pregnant with twins presenting to the general surgery clinic with abdominal pain, vomiting and a palpable abdominal mass, which eventually turned out to be a massive trichobezoar manifesting as Rapunzel syndrome. Rapunzel syndrome is a large trichobezoar extending from the stomach into the small intestine. This is perhaps the first reported case of Rapunzel syndrome in a patient pregnant with twins.

2018 Cureus

32. Intake and feed utilization in two breeds of pregnant beef cows fed forages with high-fiber concentrations Full Text available with Trip Pro

Intake and feed utilization in two breeds of pregnant beef cows fed forages with high-fiber concentrations Hereford and Charolais beef cows (n = 24 per breed) were used to study the effect of breed and to evaluate late-cut reed canarygrass (RC) and whole-crop oats plus urea (WCO) compared with late-cut timothy (TG) with respect to feed intake and digestibility, rumination time, fecal particle size (PS) distribution, N excretion, and ruminal microbial CP production (MCP). The TG and RC were cut (...) at flowering and WCO at hard dough stage of maturity. Cows were group-housed, 6 groups per breed, and fed 3 diets ad libitum in 3 periods. The study was designed as two 3 × 3 Latin squares amalgamated to form a 3 × 6 rectangle for each breed. All data were statistically analyzed on group level. Indigestible NDF (iNDF) and urinary creatinine excretion were used as markers to estimate apparent diet digestibility and daily urine volume, respectively. Fecal PS distribution was determined by dry sieving

2018 Journal of animal science

33. Gastric Barrier Dysfunction of Functional Dyspepsia and Therapeutic Response to Puyuanhewei Detected by Endomicroscopy

Gastric Barrier Dysfunction of Functional Dyspepsia and Therapeutic Response to Puyuanhewei Detected by Endomicroscopy Gastric Barrier Dysfunction of Functional Dyspepsia and Therapeutic Response to Puyuanhewei Detected by Endomicroscopy - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum (...) number of saved studies (100). Please remove one or more studies before adding more. Gastric Barrier Dysfunction of Functional Dyspepsia and Therapeutic Response to Puyuanhewei Detected by Endomicroscopy The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT02465996 Recruitment Status : Unknown Verified

2015 Clinical Trials

34. The Efficacy and Safety of Qizhiweitong Granule on Patients With Functional Dyspepsia in a Multi-center Clinical Study

severe mental disorders pregnant women, breastfeeding women or those who plan to become pregnant allergy to Qizhiweitong particle have symptoms of both subtypes of functional dyspepsia Contacts and Locations Go to No Contacts or Locations Provided More Information Go to Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number): Layout table for additonal information Responsible Party: Zhongcheng Duan, Professor, Wuhan Union Hospital, China ClinicalTrials.gov (...) The Efficacy and Safety of Qizhiweitong Granule on Patients With Functional Dyspepsia in a Multi-center Clinical Study The Efficacy and Safety of Qizhiweitong Granule on Patients With Functional Dyspepsia in a Multi-center Clinical Study - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum

2015 Clinical Trials

35. The Effect and Mechanism of Acupuncture on Functional Dyspepsia

The Effect and Mechanism of Acupuncture on Functional Dyspepsia The Effect and Mechanism of Acupuncture on Functional Dyspepsia - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. The Effect and Mechanism (...) of Acupuncture on Functional Dyspepsia The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT02358486 Recruitment Status : Recruiting First Posted : February 9, 2015 Last Update Posted : August 18, 2017 See Sponsor: Kyunghee University

2015 Clinical Trials

36. Cognitive Modulation of Dyspeptic Symptom During Food Ingestion in Functional Dyspepsia Patients Cognitive Modulation

the last 6 months certified by a medical record Exclusion Criteria: Subjects which have a non-removable metal object in or at their body, such as, for example: Heart pace-maker, Artificial heart valve, Metal prosthesis, Metallic implants (screws, plates from operations, etc.), Interuterine Spiral, Metalsplinters / grenade fragments Non-removable dental braces, Acupuncture needles, Insulin pump, Intraport, etc., Pregnant women or pregnancy cannot be excluded Nursing women Subjects with limited (...) Cognitive Modulation of Dyspeptic Symptom During Food Ingestion in Functional Dyspepsia Patients Cognitive Modulation Cognitive Modulation of Dyspeptic Symptom During Food Ingestion in Functional Dyspepsia Patients Cognitive Modulation - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number

2015 Clinical Trials

37. A Trial to Evaluate the Efficacy and Safety of YH12852 in Patients With Functional Dyspepsia

of organic lesions based on upper GI endoscopy, which could be the cause of dyspeptic symptoms Women of childbearing potential (WOCBP) must have a negative pregnancy test result at the screening visit and use an adequate method of contraception to avoid pregnancy throughout the study Exclusion Criteria: Women who are pregnant or breastfeeding. Women with a positive pregnancy test result on enrollment or prior to investigational product administration. Subjects with a history of surgery that could affect (...) A Trial to Evaluate the Efficacy and Safety of YH12852 in Patients With Functional Dyspepsia A Trial to Evaluate the Efficacy and Safety of YH12852 in Patients With Functional Dyspepsia - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more

2015 Clinical Trials

38. Efficacy of Bromopride and Simethicone Versus Bromopride in Functional Dyspepsia

Efficacy of Bromopride and Simethicone Versus Bromopride in Functional Dyspepsia Efficacy of Bromopride and Simethicone Versus Bromopride in Functional Dyspepsia - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding (...) more. Efficacy of Bromopride and Simethicone Versus Bromopride in Functional Dyspepsia The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT02604576 Recruitment Status : Recruiting First Posted : November 13, 2015 Last Update

2015 Clinical Trials

39. Functional Dyspepsia and Symptom Perception

and rivaroxaban), and clopidogrel (Patients or healthy controls using calcium carbasalate (acetylsalicylic acid 100mg 1dd1) are eligible to participate in the study. Patients or healthy controls using higher doses of calcium carbasalate will be excluded from the study). Dieting Pregnancy or lactation Smoking Excessive alcohol use (>20 alcoholic consumptions/week) and inability to avoid use of alcohol in the 2 days prior to endoscopy and multi-sugar test Functional dyspepsia patients Inclusion criteria (...) Functional Dyspepsia and Symptom Perception Functional Dyspepsia and Symptom Perception - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Functional Dyspepsia and Symptom Perception The safety and scientific

2015 Clinical Trials

40. Gastric Activity and Gastrointestinal Peptides in Patients With Functional Dyspepsia

Gastric Activity and Gastrointestinal Peptides in Patients With Functional Dyspepsia Gastric Activity and Gastrointestinal Peptides in Patients With Functional Dyspepsia - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before (...) adding more. Gastric Activity and Gastrointestinal Peptides in Patients With Functional Dyspepsia (DYSMOT-RIII) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT02113527 Recruitment Status : Completed First Posted : April 14, 2014 Last Update Posted : September 2, 2015 Sponsor: Azienda Ospedaliera

2014 Clinical Trials

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