How to Trip Rapid Review

Step 1: Select articles relevant to your search (remember the system is only optimised for single intervention studies)

Step 2: press

Step 3: review the result, and maybe amend the or if you know better! If we're unsure of the overall sentiment of the trial we will display the conclusion under the article title. We then require you to tell us what the correct sentiment is.

544 results for

Famciclovir

by
...
Latest & greatest
Alerts

Export results

Use check boxes to select individual results below

SmartSearch available

Trip's SmartSearch engine has discovered connected searches & results. Click to show

81. Efficacy and Safety of Nucleoside Antiviral Drugs for Treatment of Recurrent Herpes Labialis: A Systematic Review and Meta-Analysis. (PubMed)

of pain than did aciclovir. Both nucleoside antiviral drugs increased the percentage of aborted lesions, whereas penciclovir and famciclovir did not.Nucleoside antiviral drugs are safe and beneficial for the treatment of recurrent herpes labialis; both systemic and topical formulations are recommended. Valaciclovir is more effective than aciclovir, especially in reducing the time to healing of lesions.© 2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

2016 Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology

82. Early application of low-level laser may reduce the incidence of postherpetic neuralgia (PHN). (PubMed)

at the first, third, and sixth months after rash outbreak in 3 groups: the acute group of patients who received LLLT during the first 5 days; the subacute group of patients who received LLLT during days 6 to 14 of the eruption; and the control group of patients who did not receive LLLT.There were 48, 48, and 154 patients in the acute, subacute, and control groups, respectively. After adjusting for confounding factors, including age, sex, and use of famciclovir, the incidence of PHN was significantly lower

2016 Journal of American Academy of Dermatology

83. WITHDRAWN: Antiviral treatment for Bell's palsy (idiopathic facial paralysis).

Fergus F Somasundara Dhruvashree D Sullivan Michael M Gammie Fiona F Sullivan Frank F eng Journal Article Meta-Analysis Research Support, Non-U.S. Gov't Review Systematic Review 2015 09 07 England Cochrane Database Syst Rev 100909747 1361-6137 0 Anti-Inflammatory Agents 0 Antiviral Agents 452-06-2 2-Aminopurine 9PHQ9Y1OLM Prednisolone HG18B9YRS7 Valine MZ1IW7Q79D Valacyclovir QIC03ANI02 Famciclovir X4HES1O11F Acyclovir IM Cochrane Database Syst Rev. 2015;(7):CD001869 26130372 2-Aminopurine analogs (...) & derivatives therapeutic use Acyclovir analogs & derivatives therapeutic use Anti-Inflammatory Agents therapeutic use Antiviral Agents therapeutic use Bell Palsy drug therapy virology Drug Therapy, Combination methods Famciclovir Herpes Simplex complications drug therapy Humans Prednisolone therapeutic use Randomized Controlled Trials as Topic Treatment Outcome Valacyclovir Valine analogs & derivatives therapeutic use 2015 9 8 6 0 2015 9 8 6 0 2016 4 1 6 0 epublish 26343420 10.1002/14651858.CD001869.pub7

Full Text available with Trip Pro

2016 The Cochrane database of systematic reviews

84. Blocking virus replication during acute MCMV infection paradoxically prolongs antigen presentation and increases the CD8+ T cell response by preventing type I IFN-dependent depletion of DCs (PubMed)

Blocking virus replication during acute MCMV infection paradoxically prolongs antigen presentation and increases the CD8+ T cell response by preventing type I IFN-dependent depletion of DCs Increasing amounts of pathogen replication usually lead to a proportionate increase in size and effector differentiation of the CD8+ T cell response, which is attributed to increased Ag and inflammation. Using a murine CMV that is highly sensitive to the antiviral drug famciclovir to modulate virus

Full Text available with Trip Pro

2016 Journal of immunology (Baltimore, Md. : 1950)

85. The changing landscape of antiviral treatment of herpes zoster: a 17-year population-based cohort study (PubMed)

records were examined, and International Classification of Diseases, Ninth Revision, Clinical Modification and International Classification of Diseases, Tenth Revision, Clinical Modification codes were used to identify episodes of HZ between April 1, 1997 and March 31, 2014 in persons aged 20 or over. Annual age-adjusted incidence and hospitalization rates were calculated. Prescription records of HZ-diagnosed persons for acyclovir, valacyclovir, and famciclovir were used to calculate the rates

Full Text available with Trip Pro

2016 ClinicoEconomics and Outcomes Research: CEOR

86. Intérêt de la thérapie antivirale par voie orale dans le traitement des nécroses rétiniennes aigues (PubMed)

acuity. After the discovery of this disease using polymerase chain reaction (PCR) and immune load coefficient (ILC) usually by puncturing the cornea to evacuate the aqueous humour, the confirmation of this diagnosis allows for faster optimization of disease management decreasing the time required to confirm the diagnosis. ARN syndrome is associated with a very poor prognosis. Recent studies have shown that oral antiviral (valaciclovir, famciclovir and valganciclovir) and intravitreal therapies (...) as early as possible in order to limit bilateralization and the occurrence of complications. This study confirms that oral antiviral (valacyclovir, famciclovir and valganciclovir) and intravitreal therapies without initial intravenous treatment are an effective treatment for RNA.

Full Text available with Trip Pro

2016 The Pan African medical journal

87. [Shallow Fire-needle Acupuncture Stimulation Plus Cupping Relieves Neuralgia and Down-regulates Serum Substance P Level in Patients with Acute Herpes Zoster]. (PubMed)

in each). Patients of both groups were ordered to take Famciclovir (0.25 g/time, three times a day) and Mecobalamin (0.5 g/time, three times a day) orally for 7 days. In addition, patients of the treatment group were also treated by repeated shallow fire-needle stimulation and cupping, once a day for 7 days. Before and after the treatment, the patient's pain severity was assessed using visual analogue scale (VAS) and serum SP concentration was measured using ELISA.After the treatment, the VAS scores

2018 Zhen ci yan jiu = Acupuncture research

88. Management of STIs and related conditions in children and young people

– consider if all other treatment modalities failed Genital Herpes First episode Treat if within 5 days of start of episode or while new lesions are still developing. Child 1 month–2 years Aciclovir 100 mg orally five times a day for 5 days Child >2 years Aciclovir 200 mg orally five times a day for 5 days Recurrence If episodic or suppressive therapy is required see adult guideline. NB: Valaciclovir and famciclovir are not licensed for use in children. 45 Anogenital candidiasis Child 12 years Treatment

2010 British Association for Sexual Health and HIV

89. Immune Response to Shingles Vaccination

chickenpox or shingles in the past 5 years. VZV seronegative Taking systemic suppressive regular doses of drugs with anti-VZV activity such as acyclovir, famciclovir, or valacyclovir. Episodic use is allowed. For Cohort 1: medication cannot be taken 24 hours prior to or 30 days after receiving Zostavax per CDC recommendations. HIV seropositive. Hepatitis C infection or active Hepatitis B infection. History of a life-threatening allergic reaction (anaphylactic/anaphylactoid reaction) to gelatin, neomycin

2015 Clinical Trials

90. Safety and Effectiveness of Live Zoster Vaccine in Anti-Tumor Necrosis Factor (TNF) Users (VERVE Trial)

glucocorticoid use is prohibited for Phase Ia patients) Any known contraindication to Zostavax® vaccine, including allergy or sensitivity to gelatin or any other vaccine component Known HIV/AIDS Currently receiving radiation or chemotherapy for any type of malignancy Any current use (within the last 30 days) of acyclovir, valacyclovir, famciclovir, or foscarnet Receipt of any other immunizations within one month before study vaccination (2 weeks in the case of inactivated influenza vaccines or other non

2015 Clinical Trials

91. HSV G207 Alone or With a Single Radiation Dose in Children With Progressive or Recurrent Supratentorial Brain Tumors

involvement which would require ventricular, cerebellar or brainstem inoculation or would require access through a ventricle in order to deliver treatment Prior participant in experimental viral therapy (e.g., adenovirus, retrovirus or herpes virus protocol) Required steroid increase within 1 week prior to injection Known HIV seropositivity Concurrent therapy with any drug active against HSV (acyclovir, valaciclovir, penciclovir, famciclovir, gancyclovir, foscarnet, cidofovir) or any immunosuppressive

2015 Clinical Trials

92. Safety and PK of MBX-400 (Cyclopropavir) in Normal Volunteers

active against herpes viruses within 30 days prior to Day 1 including but not limited to: acyclovir, valacyclovir, famciclovir, penciclovir, ganciclovir and valganciclovir; 22.Use of any medication on a chronic basis; 23.Use of alcohol-containing, grapefruit-containing, or caffeine-containing foods or beverages within 72 hours prior to Check-in (Day -1); 24. Are taking or have utilized any drugs within 3 days prior to Day 1; alcohol or tobacco within 3 days prior to Day 1; or are a chronic alcohol

2015 Clinical Trials

93. Safety, Tolerability and Therapeutic Efficacy of Topical ZEP-3 Ointment (1.0%) for the Treatment of Cold Sores

-viral drug. Subject has had an infection with HSV-1 isolates know to be resistant to acyclovir, valacyclovir, famciclovir, or ganciclovir. Subject has had a herpes vaccine. Females during pregnancy, lactation or breastfeeding. Subject has a history of alcoholism or drug abuse within the preceding 12 months. Subject is currently enrolled in another clinical trial involving the use of a drug and/or a device. Any history which, in the Investigator's judgment, makes the subject ineligible or places

2015 Clinical Trials

94. Treatment of herpes zoster with ultrasound-guided superficial cervical plexus block (PubMed)

Treatment of herpes zoster with ultrasound-guided superficial cervical plexus block Herpes zoster most commonly occurs in elderly patients, and usually affects sensory neurons. Therefore, its characteristic symptoms are segmental pain, itching, and sensory changes in the affected areas. A 71-yr-old woman experienced painful herpetic rash on the right cervical 2-4 dermatomes for 16 days. Two days after the onset of the rash, she was diagnosed with herpes zoster, and prescribed 250 mg famciclovir

Full Text available with Trip Pro

2015 Journal of Dental Anesthesia and Pain Medicine

95. Postherpetic Wolf's isotopic response: Possible contribution of resident memory T cells to the pathogenesis of lichenoid reaction. (PubMed)

, Tokyo, 160-8582, Japan. Ohyama M M Department of Dermatology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582, Japan. eng Case Reports Letter 2015 10 16 England Br J Dermatol 0004041 0007-0963 0 Antigens, CD 0 Antigens, Differentiation, T-Lymphocyte 0 Antiviral Agents 0 CD69 antigen 0 Lectins, C-Type 452-06-2 2-Aminopurine QIC03ANI02 Famciclovir IM 2-Aminopurine administration & dosage analogs & derivatives Antigens, CD immunology Antigens, Differentiation, T (...) -Lymphocyte immunology Antiviral Agents administration & dosage Famciclovir Herpes Zoster drug therapy immunology pathology Humans Immunologic Memory immunology Lectins, C-Type immunology Lichenoid Eruptions etiology immunology pathology Male Middle Aged Recurrence T-Lymphocytes immunology 2015 6 27 6 0 2015 6 27 6 0 2016 10 19 6 0 ppublish 26114399 10.1111/bjd.13968

2015 British Journal of Dermatology

96. MK-8228 (Letermovir) Versus Placebo in the Prevention of Clinically-Significant Cytomegalovirus (CMV) Infection in Adult, CMV-Seropositive Allogeneic Hematopoietic Stem Cell Transplant Recipients (MK-8228-001)

allogeneic HSCT (previous autologous HSCT is acceptable) History of CMV end-organ disease within 6 months before randomization Has evidence of CMV viremia (if tested) at any time from either signing of the Informed Consent Form or the HSCT procedure, whichever is earlier, until the time of randomization. Received the following within 7 days before screening or plans to receive during the study: ganciclovir, valganciclovir, foscarnet, acyclovir, valacyclovir, or famciclovir Received the following within

2014 Clinical Trials

97. Brain Inflammation and Function in Alcoholism

that are systemic corticosteroids; antibiotics; anticholinergics; anticoagulants; anticonvulsants; antidepressants; antidiarrheal preparations; antifungal agents (systemic); antihistamines (sedating); antihypertensives; anti-inflammatory drugs (systemic); antineoplastics; antiobesity; antipsychotics; antivirals (except for treatment of HSV with agents without CNS activity, e.g. acyclovir, ganciclovir, famciclovir, valacyclovir); anxiolytics; cough/cold preparations (dextromethorphan preparations

2014 Clinical Trials

98. Dopamine Rhythms in Health and Addiction

); antianginal agents; antiarrhythmics; antiasthma agents that are systemic corticosteroids; antibiotics; anticholinergics; anticoagulants; anticonvulsants; antidepressants; antidiarrheal preparations; antifungal agents (systemic); antihistamines (sedating); antihypertensives; anti-inflammatory drugs (systemic); antineoplastics; antiobesity; antipsychotics; antivirals (except for treatment of HSV with agents without CNS activity, e.g. acyclovir, ganciclovir, famciclovir, valacyclovir); anxiolytics

2014 Clinical Trials

99. Efficacy and Safety Study of CSJ148 in Stem Cell Transplant Patients

from samples collected within 14 days prior to enrollment. Local assays could be used to qualify the patient for enrollment. Received any of the following within 30 days prior to enrollment: ganciclovir, valganciclovir, foscarnet, cidofovir, acyclovir (>25 mg/kg/day IV), valacyclovir (>3 gm/day oral), famciclovir (>1500 mg/day oral), HCMV immune globulin, immune globulin (>500 mg/kg), or any other medication with anti-HCMV activity. Required mechanical ventilation within 7 days prior to enrollment

2014 Clinical Trials

100. Acyclovir Therapy for Genital Herpes Ulcers in HIV Negative African Women

by concordant rapid testing HSV-2 seropositive (Focus HerpeSelect EIA >3.4) At least one prior occurrence of GUD 18 to 50 years of age Exclusion Criteria: Current use, or use within the past 7 days, of acyclovir, valacyclovir, or famciclovir Prior hypersensitivity and/or allergic reaction to acyclovir Use of probenecid, which prolongs renal excretion of acyclovir Current use, or use within the past 28 days, of an investigational agent Currently pregnant or nursing Currently plan to become pregnant during

2014 Clinical Trials

To help you find the content you need quickly, you can filter your results via the categories on the right-hand side >>>>