Cheap drug combo could help millions lose weight
NCT ID NCT07588750
First seen Jun 27, 2026 · Last updated Sep 03, 2026 · Updated 2 times
Summary
This study reviews medical records of 500 adults with obesity or overweight who took a combination of sibutramine and topiramate for at least three months. The goal is to see how much weight they lost and if the treatment was safe and tolerable. This is a low-cost option that may help people who cannot afford newer weight-loss drugs.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
278 people
The number who actually took part.
- Started
-
Jun 2026
- Finished
-
Sep 2026
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The study population consists of adult patients with obesity or overweight associated with metabolic comorbidities treated in a real-world outpatient clinical setting in Brazil. Participants received combined pharmacological treatment with sibutramine and topiramate during routine medical care. The population includes patients with conditions such as type 2 diabetes mellitus, prediabetes, dyslipidemia, and hypertension who underwent regular clinical follow-up with documented anthropometric and therapeutic data available in medical records for retrospective analysis.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adults aged 18 years or older at the start of treatment * Diagnosis of obesity, defined as body mass index (BMI) ≥ 30 kg/m² * Diagnosis of overweight, defined as BMI ≥ 27 kg/m², associated with at least one metabolic comorbidity, including type 2 diabetes mellitus, prediabetes, dyslipidemia, or arterial hypertension * Patients treated with concomitant sibutramine and topiramate prescribed during routine outpatient medical care * Minimum treatment duration of 3 months * At least two documented outpatient visits, including baseline and follow-up assessments * Availability of clinical and anthropometric data in the medical record, including body weight, BMI, medication dose, treatment duration, and reported adverse events * Treatment performed in an outpatient clinical setting under medical supervision Exclusion Criteria: * Pregnancy or breastfeeding during the treatment period * History of epilepsy or seizures * Severe psychiatric disorders, including schizophrenia, uncontrolled bipolar disorder, or severe depression * Significant cardiovascular disease, including previous myocardial infarction, stroke, transient ischemic attack, significant coronary artery disease, congestive heart failure, clinically relevant arrhythmias, previous deep vein thrombosis, or pulmonary embolism * Uncontrolled arterial hypertension, defined as blood pressure ≥ 160/100 mmHg during follow-up * History of nephrolithiasis * Closed-angle glaucoma or history of increased intraocular pressure associated with medication use * Severe renal or hepatic disease * Concomitant use of medications that may significantly affect body weight, including chronic corticosteroids, atypical antipsychotics, tricyclic antidepressants, other anorectic agents, or other anti-obesity medications * Incomplete medical records lacking sufficient information on body weight, BMI, medication dose, or minimum clinical follow-up * Known hypersensitivity to sibutramine, topiramate, or any component of the formulations * Treatment interruption for more than 1 month associated with weight regain
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Obesity & overweight are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Falqueto Med - N1 Centro Clínico
Venda Nova do Imigrante, Espírito Santo, 29375000, Brazil
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can cooking classes curb dangerous pregnancy weight gain?
- Do teens who know more about obesity weigh less?
- Can a starch powder trick the gut into curbing teen appetite?
- Can a Choose-Your-Own-Adventure comic help kids eat better and move more?
- Can a Weight-Loss drug and an IUD treat early uterine cancer without surgery?
- Can a Three-Part program help older adults lose fat and keep muscle?