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The Effect of Preoperative Gabapentin on Postoperative Pain Control and Analgesic Requirements Following Bariatric Surgery

A

Ain Shams University

Status

Not yet enrolling

Conditions

Bariatric Surgery Analgesia

Treatments

Drug: Group 2
Drug: Group 1

Study type

Interventional

Funder types

Other

Identifiers

NCT07169006
MD326/2024

Details and patient eligibility

About

The importance of bariatric anesthesia and analgesia research cannot be ignored as it can inform and improve the perioperative protocols for other patients with morbid obesity irrespective of the surgical procedures they are undergoing

Full description

Among various postoperative complications, pain is the main adverse event experienced by patients. Good control of postoperative pain is an important factor for reducing early postoperative complications such as pulmonary embolism, deep vein thrombosis, ileus, and respiratory infections, and for decreasing length of stay, lowering costs, and increasing patient satisfaction

Enrollment

102 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients with American Society of Anesthesiologists physical status ASA I to III
  • both genders
  • Morbid obese scheduled for bariatric surgery

Exclusion criteria

  • patients with impaired liver or kidney disease
  • patients with history of hypersensitivity to gabapentin
  • patients with history of alcohol abuse, chronic pain or frequent use of analgesic
  • patients with uncontrolled medical disease

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

102 participants in 2 patient groups, including a placebo group

Group 1
Experimental group
Description:
Will receive a single dose of gabapentin 300 mg preoperatively before standard general anesthesia
Treatment:
Drug: Group 1
Group 2
Placebo Comparator group
Description:
will receive a placebo before standard general anesthesia
Treatment:
Drug: Group 2

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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