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Completed

NCT Number: NCT06254183

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

Assessment of the effect of gabapentin as an analgesic replacement on the Kidney function following Laparoscopic sleeve gastrectomy for Morbid Obese Patients by measuring two biomarkers: NGAL (Neutrophil gelatinase-associated lipocalin)and DKK3 (Dickkopf-3)

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Key information

About this study

Obesity should be viewed as the number one preventable risk factor for kidney disease because obesity mediates the majority of diabetes and hypertension, the 2 major causes of end-stage kidney disease (ESKD). Morbidly obese adults have a 6-fold higher risk of diabetes compared with their lean peers.

Laparoscopic sleeve gastrectomy (LSG) has been approved since 2010, by both the American Society for Metabolic and Bariatric Surgery (ASMBS) and the American College of Surgeons (ACS) as an operation for the treatment of obesity and other obesity-related diseases.

Acute kidney injury (AKI) is one of the most common postoperative complications. It is a serious morbidity occurring during hospitalizations, and it is associated with prolonged hospital stay, high risk of in-hospital mortality, increased hospital costs, and decreased survival for up to 15 years after surgery. In addition, AKI increases the risk of incident and progressive chronic kidney disease and is associated with reduced long-term survival.

Non-steroidal anti-inflammatory drugs (NSAIDs) represent one of the most common classes of medications used postoperatively. It is estimated that 1-5% of NSAIDs users may develop renal adverse effects, both AKI and CKD.

Gabapentin, an anticonvulsant widely used for the treatment of various neuropathic pain syndromes, has recently been investigated as an analgesic agent in the perioperative setting. Although it is not an analgesic itself, early experience suggests this medication can improve pain and reduce opioid requirements.

A new animal study shows that gabapentin demonstrated reno-protective properties against either acute or chronic kidney injury, primarily attributed to its antioxidant properties. Further clinical studies are required to validate and standardize therapeutic doses of gabapentin under investigation in patients susceptible or at risk of developing kidney dysfunction.

In this study, Neutrophil gelatinase-associated lipocalin (NGAL) and Dickkopf-3 (DKK3) will be biomarkers to assess kidney function. NGAL appears to be a promising marker for early detection of AKI and is likely to be adapted for wide-scale clinical use in patient management as a point-of-care test.

Measurement of DKK3 in urine represents a novel tool for the identification of patients at high risk for AKI regardless of the cause of kidney injury.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Morbid obese patients with normal kidney function, undergoing Laparoscopic sleeve gastrectomy surgery.
  • Both sexes.
  • Age ≥ 18 years

Exclusion criteria

  • • Patients have advanced cancer on active treatment and end-stage renal, hepatic, and cardiopulmonary disease.
  • Patients with untreated schizophrenia, cognitive impairment and using psychiatric medications.
  • Patients with active substance abuse.
  • Patients on chronic dosage of Gabapentin or allergic to it.
  • Pregnant women or women on breastfeeding.
  • Patients on medications that could interfere with assessed parameters will be excluded.

The ethical approval of the study will be obtained from by Medical research Ethics Committee of Tanta and Mansoura Universities and all participants will give their written consent.

Treatment and study plan

Laparoscopic sleeve gastrectomy

Procedure

Standard laparoscopic sleeve gastrectomy performed under general anesthesia according to institutional protocol, with gastric resection over a calibration bougie.

Other names: Bariatric Surgery, LSG, Sleeve Gastrectomy

gabapentin 1200 mg

Drug

A single oral dose of 1200 mg gabapentin administered 1 hour prior to induction of anesthesia for laparoscopic sleeve gastrectomy. The medication is given as two 600 mg tablets ((Unipharma Co.)

Other names: Neurontin

Primary outcomes

  1. Change in renal function markers (serum creatinine and BUN) from baseline

    Time frame: Baseline,24 hours postoperatively and 6 months after surgery

    Serum creatinine (mg/dL) and blood urea nitrogen, BUN (mg/dL) measured preoperatively (baseline) and at 24 hours after laparoscopic sleeve gastrectomy; primary analysis is the change from baseline to 24 hours postoperatively.

Secondary outcomes

  1. Level of NGAL

    Time frame: Baseline, 24 hours postoperatively and 6 months after surgery

    Serum NGAL measured by ELISA kit

  2. Level of Dickkopf-3 (DKK3)

    Time frame: Baseline,24 hours postoperatively and 6 months after surgery

    Serum and urine DKK3 measured by ELISA kit

Other outcomes

  1. Change in lipid profile from baseline

    Time frame: Baseline and 6 months after surgery

    Total cholesterol, LDL-C, HDL-C, and triglycerides measured preoperatively (baseline) and at 6 months postoperatively; change from baseline to 6 months.

  2. Serum calcium level

    Time frame: Baseline, 24 hours postoperatively and 6 months

    Serum calcium (mg/dL) measured preoperatively (baseline) and at 24 hours after surgery to assess concomitant electrolyte/metabolic factors that may be associated with postoperative renal dysfunction.

  3. Serum uric acid level

    Time frame: Baseline,24 hours postoperatively and 6 months after surgery

    Serum uric acid (mg/dL) measured preoperatively (baseline) and at 24 hours after surgery to assess concomitant metabolic factors that may be associated with postoperative renal dysfunction.

Sponsors and collaborators

Lead sponsor

Tanta University

Other

Registry information

Official study title

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

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Feb 12, 2024
Registry last updated
Feb 25, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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