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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05533684
Other study ID # 343-2022
Secondary ID
Status Completed
Phase Early Phase 1
First received
Last updated
Start date September 1, 2022
Est. completion date December 31, 2022

Study information

Verified date March 2023
Source Minia University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Single dose 600 mg gabapentin will be given preoperatively in anal surgeries


Description:

Patients will be grouped into 2 groups of 25 patients each, the first group will receive 600 mg of gabapentin one hour before surgery and the second group will receive a placebo tablet. pain scores will be measured postoperatively


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date December 31, 2022
Est. primary completion date December 31, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: 1. ASA physical status I or II 2. Aged from 18 to 65 years 3. Scheduled for anal surgeries at Minya University Hospital Exclusion Criteria: 1. Presence of contraindications to neuraxial anesthesia 2. Presence of history of central nervous system or mental disorders, epilepsy, chronic pain, or drug abuse. 3. The use of neuropathic analgesic or antiepileptic drugs

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Gabapentin
single preoperative dose of 600 mg gabapentin

Locations

Country Name City State
Egypt Sarah Omar Minya

Sponsors (1)

Lead Sponsor Collaborator
Minia University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary postoperative pain measuring postoperative pain using the visual analog scale from 0 to 10, where zero is the least, and 10 is the worst pain first 12 hours postoperative
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