A Single Preoperative Dose of Gabapentin to Decreases Postoperative Pain in Ambulatory Anal Surgeries

M

Minia University

Status and phase

Completed
Early Phase 1

Conditions

Pain, Postoperative

Treatments

Drug: Gabapentin

Study type

Interventional

Funder types

Other

Identifiers

NCT05533684
343-2022

Details and patient eligibility

About

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

Full 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

Enrollment

50 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ASA physical status I or II
  • Aged from 18 to 65 years
  • Scheduled for anal surgeries at Minya University Hospital

Exclusion criteria

  • Presence of contraindications to neuraxial anesthesia
  • Presence of history of central nervous system or mental disorders, epilepsy, chronic pain, or drug abuse.
  • The use of neuropathic analgesic or antiepileptic drugs

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

50 participants in 2 patient groups

postoperative pain
No Intervention group
Description:
Measuring postoperative pain using the visual analogue scale
total analgesic consumption
Other group
Description:
Recording the total amount of analgesia consumed by the patients
Treatment:
Drug: Gabapentin

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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