Fact CheckerSign in

NCT06254183CompletedPhase 4

Effect of Gabapentin on Kidney Function Following Laparoscopic Sleeve Gastrectomy (LSG)

Clinical Study Evaluating the Effect of Gabapentin on Kidney Function Following Laparoscopic Sleeve Gastrectomy (LSG) for Morbid Obese Patients

Source: ClinicalTrials.gov · Last updated 18 Aug 2026

Brief summary (registry, in English)

This study evaluated the effect of a single preoperative dose of gabapentin on renal stress and kidney function following laparoscopic sleeve gastrectomy in adults with severe obesity. Sixty participants undergoing laparoscopic sleeve gastrectomy were randomized in a 1:1 ratio to surgery without preoperative gabapentin or surgery after a single 1200-mg oral dose of gabapentin. An additional 30 non-operative participants with severe obesity served as a non-randomized external reference cohort. Renal assessment included conventional kidney function markers and biomarkers, including Dickkopf-3 (DKK3) and neutrophil gelatinase-associated lipocalin (NGAL). The prespecified primary endpoint was urinary DKK3 concentration at 24 hours postoperatively.

Status (registry)
Completed
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
90 (actual)
First submitted
22 Jan 2024
Start date
1 Dec 2024
Primary completion date
1 May 2025
Lead sponsor
Tanta University
Diseases
Obesity
NCT number
NCT06254183

What you commit to

  • Study type: Interventional · Phase 4
  • Participants enrolled: 90
  • From 1 Dec 2024 to the primary completion date, 1 May 2025
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Advanced cancer receiving active treatment.
  • Use of medications that could interfere with the assessed study parameter

Other illness

  • End-stage renal, hepatic, or cardiopulmonary disease.
  • Untreated schizophrenia or cognitive impairment.
  • Use of psychiatric medications, as specified in the study protocol.
  • Chronic use of gabapentin or known hypersensitivity to gabapentin.

Other

  • Active substance abuse.
  • Pregnancy or breastfeeding.

Who the study is looking for

  • Age: 18-65 years old.
  • Participants with severe obesity (BMI ≥40 kg/m², without comorbidities or BMI ≥35 kg/m², in the presence of obesity-related comorbidities).
  • Preserved kidney function at baseline.
  • For the randomized surgical cohort (Groups II and III), participants with severe obesity scheduled to undergo laparoscopic sleeve gastrectomy.
  • For the non-randomized external reference cohort (Group I), participants with severe obesity who did not undergo laparoscopic sleeve gastrectomy during the study period or receive the study intervention.
  • Both sexes.

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Mansoura University Hospitals
Coordinator of this site? Confirm its status
Al MansurahEgyptUnknown status
Tanta University Hospitals
Coordinator of this site? Confirm its status
TantaEgyptUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.