Clinical Trials Directory

Trials / Completed

CompletedNCT03809702

Efficacy of Pregabalin for the Treatment of Acute Herpetic Neuralgia

Efficacy of Pregabalin for the Treatment of Acute Herpetic Neuralgia and for the Prevention of Post Herpetic Neuralgia- a Randomized Controlled Trial

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
82 (actual)
Sponsor
B.P. Koirala Institute of Health Sciences · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

All eligible Herpes Zoster patients will be randomized into two groups. Group 1 will be the treatment group receiving Pregabalin 75 mg twice daily for 4 weeks in addition to other routine treatment. Whereas, group 2 will be the control group receiving all routine treatment similar to group 1 except Pregabalin. Instead control group will receive Placebo.

Detailed description

This study wants to see the role of Pregabalin in acute herpetic neuralgia pain reduction and for the prevention of post herpetic neuralgia incidence as compared to placebo group. For this purpose, all eligible Herpes Zoster patients will be randomized into two groups (41 patients in each group i.e.82 total patients). Group 1 will be the treatment group receiving Pregabalin 75 mg twice daily for 4 weeks in addition to other routine treatment. Whereas, group 2 will be the control group receiving all routine treatment similar to group 1 except Pregabalin. Instead of pregabalin, control group will receive Placebo. The pain will be evaluated in all patients in each follow visits (weekly follow up for 4 weeks then monthly follow up for next three months). If it is difficult for the patient to present physically, telephonic follow up will be done to find the pain score in the required time. Also, DLQI (Dermatological life quality index) will be assessed at the first and last visit of the patient. At the end, pain score will be compared between the two groups.

Conditions

Interventions

TypeNameDescription
DRUGPregabalinPain score in group 1 (intervention group) will be compared with pain score in group 2 (placebo group)
DRUGPlaceboPain score in group 1 (intervention group) will be compared with pain score in group 2 (placebo group)

Timeline

Start date
2018-07-15
Primary completion
2019-09-20
Completion
2019-12-30
First posted
2019-01-18
Last updated
2020-10-14

Locations

1 site across 1 country: Nepal

Source: ClinicalTrials.gov record NCT03809702. Inclusion in this directory is not an endorsement.