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81. Surviving and fatal Elephant Endotheliotropic Herpesvirus-1A infections in juvenile Asian elephants – lessons learned and recommendations on anti-herpesviral therapy (PubMed)

Surviving and fatal Elephant Endotheliotropic Herpesvirus-1A infections in juvenile Asian elephants – lessons learned and recommendations on anti-herpesviral therapy Elephant Endotheliotropic Herpesviruses (EEHVs) can cause acute haemorrhagic disease in young Asian elephants (Elephas maximus) and clinical EEHV infections account for the majority of their fatalities. The anti-herpesviral drug famciclovir (FCV) has been used routinely to treat viraemic at-risk elephants, but thus far without

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2016 BMC veterinary research

82. Clinical study of Gene-Eden-VIR/Novirin in genital herpes: suppressive treatment safely decreases the duration of outbreaks in both severe and mild cases (PubMed)

better than those reported in the studies that tested acyclovir, valacyclovir, and famciclovir. The current paper reports the effect of suppressive treatment with Gene-Eden-VIR/Novirin on the duration of outbreaks, in severe and mild genital herpes cases.The framework was a retrospective chart review. The population included 137 participants. The treatment was 1-4 capsules per day. The duration of treatment was 2-48 months. The study included three controls: baseline, no-treatment, and dose

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2016 Clinical and translational medicine

83. A Long-term Follow-up Study (ZOE-LTFU) of Two Studies 110390 (ZOSTER-006) and 113077 (ZOSTER-022) to Assess the Efficacy, Safety, and Immunogenicity Persistence of GSK Biologicals' Herpes Zoster Subunit (HZ/su) Vaccine and Assessment of 1 or 2 Additional

of immunoglobulins and/or any blood products within 3 months prior to Visit Month 0 of study ZOSTER-049 or planned administration during the study period. Prolonged use (> 14 consecutive days) of oral and/or parenteral antiviral agents that are active against VZV (acyclovir, valacyclovir, famciclovir, etc. ) and planned to be used during the study period for an indication other than to treat suspected or confirmed HZ or an HZ-related complication (topical use of these antiviral agents is allowed). Important

2016 Clinical Trials

84. Prospective Evaluation of Adjusted Body Weight Dosing of Acyclovir in Obesity

mg/kg (TBW for normal weight patients and ABW40 for obese patients) as part of their routine care Weight > 190% of ideal body weight (IBW) for "obese" patients or weight 80-120% of IBW for matched control patients. Exclusion Criteria: Receipt of acyclovir or a pro-drug of acyclovir (valacyclovir, ganciclovir, valganciclovir, famciclovir) in the prior 24 hours Serum creatinine >1.5 mg/dL Hypersensitivity to acyclovir Patients requiring ventilator support or vasopressors in the prior 24 hours

2016 Clinical Trials

85. 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

86. 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

87. 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

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2016 The Cochrane database of systematic reviews

88. 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

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

89. 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

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2016 ClinicoEconomics and Outcomes Research: CEOR

90. 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.

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2016 The Pan African medical journal

91. [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

92. 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

93. 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

94. 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

95. 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

96. 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

97. 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

98. 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

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2015 Journal of Dental Anesthesia and Pain Medicine

99. 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

100. 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

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