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Cheap drug combo could help millions lose weight

NCT ID NCT07588750

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

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

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Conditions

The condition(s) this trial relates to.

Obesity obesity disorder Overweight

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.