Proof-of-concept trial on the efficacy of sodium tungstate in human obesity

Diabetes Obes Metab. 2010 Nov;12(11):1013-8. doi: 10.1111/j.1463-1326.2010.01293.x.

Abstract

Aim: Considering the poor long-term success of current dietary and pharmacological interventions, we aimed to evaluate the potential effect of sodium tungstate in the treatment of grade I and II obesity (ClinicalTrials.gov identifier: NCT00555074).

Methods: Prospective, randomized, placebo-controlled, double-blind, proof-of-concept study was carried out. Following a 2-week lead-in period, 30 obese (body mass index, BMI 30.0-39.9 kg/m(2)), non-diabetic subjects were randomized to receive either sodium tungstate (100 mg bid) or placebo for 6 weeks. The primary study endpoint was the absolute change in body weight relative to the time of randomization.

Results: Treatment with sodium tungstate [-0.135 ± 0.268 kg (95% CI -0.686 to +0.416 kg)] was not associated with a significant weight loss compared to placebo [-0.063 ± 0.277 kg (95% CI -0.632 to +0.507 kg)] (p = 0.854). Likewise, treatment with sodium tungstate was not associated with significant changes in fat mass (DEXA), resting energy expenditure (indirect calorimetry) or caloric consumption (3-day food records).

Conclusion: Our data do not support sodium tungstate as a pharmacological agent in the treatment of human obesity.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Anti-Obesity Agents / administration & dosage*
  • Anti-Obesity Agents / pharmacology
  • Body Mass Index
  • Double-Blind Method
  • Female
  • Humans
  • Male
  • Middle Aged
  • Obesity / complications
  • Obesity / drug therapy*
  • Placebos / administration & dosage
  • Prospective Studies
  • Treatment Outcome
  • Tungsten Compounds / pharmacology
  • Tungsten Compounds / therapeutic use*
  • Weight Loss / drug effects*

Substances

  • Anti-Obesity Agents
  • Placebos
  • Tungsten Compounds
  • sodium tungstate(VI)

Associated data

  • ClinicalTrials.gov/NCT00555074