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Headache in Pregnancy

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141. Specific Neck Rehabilitation for Unilateral Neck Related Headache and Structural Changes in the Brain

Specific Neck Rehabilitation for Unilateral Neck Related Headache and Structural Changes in the Brain Specific Neck Rehabilitation on Patients With Cervicogenic Headache, and Structural and Functional Changes in the Brain - 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. Specific Neck Rehabilitation on Patients With Cervicogenic Headache, and Structural and Functional Changes in the Brain 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

2016 Clinical Trials

142. Comparison of Two Detoxification Protocols for Treatment of Medication-overuse Headache

Pregnancy or breastfeeding Inadequate language skills to follow the patient education and filling out questionnaires. Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor. Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02903329 Locations Layout table for location information Denmark Danish Headache Center (...) Comparison of Two Detoxification Protocols for Treatment of Medication-overuse Headache Comparison of Two Detoxification Protocols for Treatment of Medication-overuse Headache - 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

2016 Clinical Trials

143. Role of Prophylaxis by Oral Fluid Supplementation in Prevention of Postdural Puncture Headache

Role of Prophylaxis by Oral Fluid Supplementation in Prevention of Postdural Puncture Headache Role of Prophylaxis by Oral Fluid Supplementation in Prevention of Postdural Puncture Headache - 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. Role of Prophylaxis by Oral Fluid Supplementation in Prevention of Postdural Puncture Headache (PROPHYDRA) 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: NCT02859233 Recruitment Status : Unknown Verified February 2017 by Nantes University Hospital. Recruitment status

2016 Clinical Trials

144. Evaluation of the Effectiveness and Tolerance of Tetracosactide Synacthen® in the Treatment of Post Dural Puncture Headaches (ESYBRECHE)

Evaluation of the Effectiveness and Tolerance of Tetracosactide Synacthen® in the Treatment of Post Dural Puncture Headaches (ESYBRECHE) Evaluation of the Effectiveness and Tolerance of Tetracosactide Synacthen® in the Treatment of Post Dural Puncture Headaches (ESYBRECHE) - 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. Evaluation of the Effectiveness and Tolerance of Tetracosactide Synacthen® in the Treatment of Post Dural Puncture Headaches (ESYBRECHE) (ESYBRECHE) 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

2016 Clinical Trials

145. Circadian Rhythm and Attack-timing in Episodic Cluster Headache Patients in- and Outside of Bout: an Actigraphic Study

medication within 2 weeks before the study initiation and during the 2 weeks. Serious somatic and/or psychiatric disorders Alcohol intake > 50 units pr.week Pregnancy / breastfeeding Patient cannot accept the conditions of the trial Patient does not understand Danish. CONTROLS Inclusion Criteria: - Age between 18 and 65 years of age Exclusion Criteria: Circumstances, determined by the PI, that makes the patient ineligible. Any primary headache more than 1 day / month Diagnosed with a secondary headache (...) Circadian Rhythm and Attack-timing in Episodic Cluster Headache Patients in- and Outside of Bout: an Actigraphic Study Circadian Rhythm and Attack-timing in Episodic Cluster Headache Patients in- and Outside of Bout: an Actigraphic 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

2016 Clinical Trials

146. Olanzapine for Acute Headaches

Volunteers: Yes Criteria Inclusion Criteria: Adult patient between 18-65 years of age presenting to the emergency department with acute primary headache Patient approved for inclusion by primary attending physician in the emergency department Exclusion Criteria: Age < 18 or > 65 Pregnancy Known allergy to olanzapine Known QT prolongation or underlying condition that places patient at risk for QT prolongation Inability to give written consent (intoxication, altered mental status) Headache of organic (...) Olanzapine for Acute Headaches Olanzapine for Acute Headaches - 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. Olanzapine for Acute Headaches (Olanzapine) The safety and scientific validity of this study

2016 Clinical Trials

147. Prazosin for Post-Concussive Headaches

Prazosin for Post-Concussive Headaches Prazosin for Post-Concussive Headaches - 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. Prazosin for Post-Concussive Headaches The safety and scientific validity (...) brain injuries, people with mTBI can have problems with their memory and concentration. People with mTBI can also find they are more irritable, have more anxiety, and have trouble with their mood and sleep. The purpose of this study is to see if a medication called prazosin can help treat chronic headaches in people with mTBI. The Food and Drug Administration (FDA) has approved prazosin for treating people with high blood pressure. At this time, the FDA has not approved prazosin in the treatment

2016 Clinical Trials

148. Efficacy of Haloperidol vs. Metoclopramide for Treatment of Acute Headaches and Migraines in the Emergency Department

may contact the study research staff using the contacts provided below. For general information, Layout table for eligibility information Ages Eligible for Study: 18 Years and older (Adult, Older Adult) Sexes Eligible for Study: All Accepts Healthy Volunteers: No Criteria Inclusion Criteria: Patients who present with a headache or migraine with onset less than or equal to 72 hours Exclusion Criteria: Known pregnancy Breast-feeding women Known history of arrhythmias or QT prolongation (450 ms (...) Efficacy of Haloperidol vs. Metoclopramide for Treatment of Acute Headaches and Migraines in the Emergency Department Efficacy of Haloperidol vs. Metoclopramide for Treatment of Acute Headaches and Migraines in the Emergency Department - 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

2016 Clinical Trials

149. Is Detoxification Needed in Medication-overuse Headache?

. Exclusion Criteria: Severe physical illness or psychiatric disorders. Addiction to alcohol or other drugs. Current treatment with headache prophylaxis. Patients can be included minimum 5 weeks after stop of prophylaxis. Pregnancy, breastfeeding or planned pregnancy within the next 12 months. Inability to provide reliable information about medical history. Criteria for Control group 1 - Episodic migraineurs: Episodic migraine, with/without concomitant tension-type headache, according to the ICHD-III beta (...) . Headache days / month ≤ 6 at time of inclusion. Days with analgesics / month ≤ 6 at time of inclusion. Prophylactics are allowed. Age ≥ 18 years old. Ability to fill out headache calendar. No previous medication overuse. No significant co-morbid pain, physical or psychiatric disorders. No addiction to alcohol or drug-abuse. No pregnancy, breastfeeding or planned pregnancy within the next 12 months. Criteria for Control group 2 - Healthy volunteers: •≥ 2 days with headache in the past month at time

2016 Clinical Trials

150. Hypertension in pregnancy: diagnosis and management

-eclampsia who did not take antihypertensive treatment and have given birth, start antihypertensive treatment if blood pressure is 150/ 100 mmHg or higher. Hypertension in pregnancy: diagnosis and management (CG107) © NICE 2018. All rights reserved. Subject to Notice of rights (https://www.nice.org.uk/terms-and- conditions#notice-of-rights). Page 22 of 491.5.3.3 Ask women with pre-eclampsia who have given birth about severe headache and epigastric pain each time blood pressure is measured. 1.5.3.4 (...) setting if birth is planned within 24 hours. 1.8.1.3 If considering magnesium sulphate* treatment, use the following as features of severe pre-eclampsia: Hypertension in pregnancy: diagnosis and management (CG107) © NICE 2018. All rights reserved. Subject to Notice of rights (https://www.nice.org.uk/terms-and- conditions#notice-of-rights). Page 28 of 49severe hypertension and proteinuria or or mild or moderate hypertension and proteinuria with one or more of the following: symptoms of severe headache

2010 National Institute for Health and Clinical Excellence - Clinical Guidelines

151. Post-dural Puncture Headache: A Comparison Between Median and Paramedian Approaches in Orthopedic Patients. (PubMed)

Post-dural Puncture Headache: A Comparison Between Median and Paramedian Approaches in Orthopedic Patients. Post-dural puncture headache (PDPH) is an iatrogenic complication of spinal anesthesia. Reported risk factors for PDPH include sex, age, pregnancy, needle tip shape and size, bevel orientation, approach and others. Little is known regarding the effect of different approaches on the incidence of PDPH.In this study we aimed to compare the incidence of PDPH in the case of median

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2015 Anesthesiology and pain medicine Controlled trial quality: uncertain

152. Safety and Efficacy Study of SOM230 s.c. in Cluster Headache

Safety and Efficacy Study of SOM230 s.c. in Cluster Headache Safety and Efficacy Study of SOM230 s.c. in Cluster Headache - 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. Safety and Efficacy Study of SOM230 (...) s.c. in Cluster Headache 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: NCT02619617 Recruitment Status : Terminated (Non-efficacy in first Phase 2a cohort.) First Posted : December 2, 2015 Last Update Posted : February 18, 2019 Sponsor: Novartis Pharmaceuticals Information provided by (Responsible

2015 Clinical Trials

153. Pilot Study of DFN-11 Injection in Medication Overuse Headache

Pilot Study of DFN-11 Injection in Medication Overuse Headache Pilot Study of DFN-11 Injection in Medication Overuse Headache - 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. Pilot Study of DFN-11 Injection (...) in Medication Overuse Headache 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: NCT02583425 Recruitment Status : Terminated First Posted : October 22, 2015 Results First Posted : April 3, 2018 Last Update Posted : April 3, 2018 Sponsor: Dr. Reddy's Laboratories Limited Information provided by (Responsible Party

2015 Clinical Trials

154. Sodium Oxybate in Patients With Episodic and Chronic Cluster Headache

Sodium Oxybate in Patients With Episodic and Chronic Cluster Headache Sodium Oxybate in Patients With Episodic and Chronic Cluster Headache - 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. Sodium Oxybate (...) in Patients With Episodic and Chronic Cluster Headache (SOinCH) 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: NCT02637648 Recruitment Status : Unknown Verified December 2015 by Ramin Khatami, Klinik Barmelweid. Recruitment status was: Not yet recruiting First Posted : December 22, 2015 Last Update Posted

2015 Clinical Trials

155. Cognitive-Behavior Therapy for Posttraumatic Headache

] they are pregnant or plan to become pregnant during the trial (due to concerns about pregnancy-induced headache that may obscure findings) if a psychiatric problem is present that warrants immediate treatment based upon clinical judgment if they demonstrate significant cognitive impairment that could impact treatment adherence/benefit. Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using (...) Cognitive-Behavior Therapy for Posttraumatic Headache Cognitive-Behavior Therapy for Posttraumatic Headache - 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. Cognitive-Behavior Therapy for Posttraumatic

2015 Clinical Trials

156. The Effect of Sumatriptan and Placebo on Isosorbide-5-mononitrate Induced Headache

headache society (IHS) criteria for migraine with or without aura of both sexes 18-70 years 45-95 kg. Exclusion Criteria: Healthy: Any type of headache (except episodic tension-type headache < 1 day per week) Serious somatic or psychiatric disease Pregnancy Intake of daily medication (except oral contraceptives). Migraine patients: Any other type of headache then migraine without aura (except episodic tension-type headache < 1 day per week) Serious somatic or psychiatric disease Pregnancy, and intake (...) The Effect of Sumatriptan and Placebo on Isosorbide-5-mononitrate Induced Headache The Effect of Sumatriptan and Placebo on Isosorbide-5-mononitrate Induced Headache - 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

2015 Clinical Trials

157. The Effect of Sumatriptan and Placebo on Cilostazol Induced Headache

meet IHS criteria for migraine with or without aura of both sexes 18-70 years 45-95 kg. Exclusion Criteria: Healthy: Any type of headache (except episodic tension-type headache < 1 day per week) Serious somatic or psychiatric disease Pregnancy Intake of daily medication (except oral contraceptives). Migraine patients: Any other type of headache then migraine without aura (except episodic tension-type headache < 1 day per week) Serious somatic or psychiatric disease Pregnancy Intake of daily (...) The Effect of Sumatriptan and Placebo on Cilostazol Induced Headache The Effect of Sumatriptan and Placebo on Cilostazol Induced Headache - 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

2015 Clinical Trials

158. Drinking Extra Water for to Prevent or Decrease Headaches

Drinking Extra Water for to Prevent or Decrease Headaches Drinking Extra Water for to Prevent or Decrease Headaches - 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. Drinking Extra Water for to Prevent (...) or Decrease Headaches 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: NCT02330809 Recruitment Status : Not yet recruiting First Posted : January 5, 2015 Last Update Posted : February 26, 2018 See Sponsor: ThinkWell Information

2014 Clinical Trials

159. Feasibility Study of Normobaric Oxygen Delivered by a High Flow Concentrator in the Treatment of Chronic Headache

treatment or same prophylaxis treatment from more than one month Signed informed consent Exclusion Criteria: Pregnancy One or more failed withdrawal treatment analgesic treatment for another reason than headache Contraindication of normobaric oxygen therapy Contraindication of ketoprofen (rescue therapy) Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information (...) Feasibility Study of Normobaric Oxygen Delivered by a High Flow Concentrator in the Treatment of Chronic Headache Feasibility Study of Normobaric Oxygen Delivered by a High Flow Concentrator in the Treatment of Chronic Headache - 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

2014 Clinical Trials

160. Exercise in Migraine and Co-existing Tension-type Headache and Neck Pain

using the contacts provided below. For general information, Layout table for eligibility information Ages Eligible for Study: 18 Years to 65 Years (Adult, Older Adult) Sexes Eligible for Study: All Accepts Healthy Volunteers: No Criteria Inclusion Criteria: Migraine Tension-type headache Neck pain Exclusion Criteria: Whiplash injury or other significant neck trauma Nerve root compression Post traumatic headache Medication overuse headache Cluster headache Trigeminal neuralgia Pregnancy and breast (...) Exercise in Migraine and Co-existing Tension-type Headache and Neck Pain Exercise in Migraine and Co-existing Tension-type Headache and Neck Pain - 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. Exercise

2014 Clinical Trials

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