Clinical trials

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Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Cohort Study of Metabolic Disease and Hypertension

The goal of this observational study is to learn how type 2 diabetes and high blood pressure develop over time in adults in Mexico. The study will include men and women between 18 and 65 years of age who do not have a previous diagnosis of these conditions. The main questions this study aims to answer are: What factors increase the risk of developing type 2 diabetes? What factors increase the risk of developing high blood pressure? Participants will not receive any experimental treatment. Researchers will observe their health as part of their regular medical care. Participants will: Attend an initial visit that includes physical measurements, blood tests, and questionnaires about their health, lifestyle, and environment Perform a simple walking test to measure physical fitness Return once a year for follow-up visits over a period of five years During the study, researchers will monitor participants to identify new cases of type 2 diabetes and high blood pressure. The results of this study may help improve prevention strategies and support public health programs aimed at reducing chronic diseases in Mexico.

Participants needed: 2,500
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Coordinación de Investigación en Salud, MexicoUpdated: May 11, 2026Locations: 1Duration: 5 Years
Eligibility criteria

Adults aged 18 to 65 years [+4]

Prior diagnosis of type 2 diabetes mellitus or hypertension [+3]

Status: Recruiting

Telerehabilitation Program to Improve Function in People With Chronic Low Back Pain Compared With Conventional Care

The goal of this clinical trial is to evaluate whether an additional telerehabilitation program, combined with conventional care, can improve functional recovery in adults with chronic low back pain treated in primary care clinics of the Mexican Institute of Social Security (IMSS). The main questions it aims to answer are: * Does the telerehabilitation program lead to greater functional improvement, measured by the Oswestry Disability Index (ODI), compared with conventional care alone? * Does the program reduce pain intensity and improve adherence and satisfaction among participants? Researchers will compare patients receiving conventional care plus telerehabilitation with those receiving conventional care only to determine whether the digital intervention provides additional clinical benefits. Participants will: * Continue their usual medical care for chronic low back pain at IMSS clinics. * Follow a 6-week telerehabilitation program delivered through an online platform, including educational videos, stretching and strengthening exercises, and weekly virtual check-ins. * Complete baseline and post-intervention assessments of pain, disability, and satisfaction.

Participants needed: 200
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: Coordinación de Investigación en Salud, MexicoUpdated: Nov 25, 2025Locations: 1
Eligibility criteria

Adults between 18 and 60 years of age. [+6]

Specific causes of low back pain (e.g., fractures, tumors, infections, inflammat... [+6]

Status: Recruiting

Efficacy of Fistulotomy for Biliary Cannulation

Access to the main bile duct is the first step in order to perform a therapeutic maneuver for biliary diseases. Early precut has been shown to ameliorate cannulation success rate, specially in difficult cannulation cases, when compared to guidewire cannulation (which is considered, for most, the standard technique). We aim to perform a randomized clinical trial comparing fistulotomy (F) precut vs guidewire cannulation (CC), as a primary cannulation technique, and compare outcomes between high experienced endoscopists (\> 200 ERCPs\[Endoscopic Retrograde cholangiopancreatography\]) and low experienced endoscopists (\< 200 ERCPs).

Participants needed: 320
Trial details
Age: 18-90Biological sex: AllType: InterventionalSponsor: Coordinación de Investigación en Salud, MexicoUpdated: May 1, 2025Locations: 1
Eligibility criteria

All patients undergoing ERCP with suspected or confirmed of choledocholithiasis,...

patients with previous ERCP, altered gastro-duodenal anatomy by previous surgery...

Status: Recruiting

Efficacy and Safety of Vitamin D Supplementation in Pediatric Patients with Obesity

Introduction: Vitamin D deficiency is commonly observed in patients with obesity, primarily due to sequestration by adipose tissue. Recent research highlights the importance of this deficiency, showing a correlation between low vitamin D levels and mechanisms contributing to insulin resistance. Objectives: This study aims to compare the effects of supplementing with 4,000 IU of vitamin D versus 1,000 IU over six months on insulin resistance and the leptin/adiponectin ratio in school-aged children and adolescents with obesity. Materials and Methods: A controlled clinical trial will be conducted involving 40 children with obesity aged 10 to 18 years (BMI \>95th percentile). Participating children and their parents will undergo measurements such as weight, height, BMI, body fat, and Tanner stage. All participants will receive dietary and physical activity recommendations based on WHO guidelines. After initial assessments, participants will be randomly assigned to receive either 4,000 IU or 1,000 IU of vitamin D. They will be monitored monthly for capsule intake and adverse effects, with follow-up measurements of anthropometry, leptin, adiponectin, insulin \& lipid profile. Statistical Analysis: Baseline characteristics will be compared using t-Student or U-Mann Whitney tests, depending on variable distribution. The intervention's impact will be assessed by calculating deltas for body fat and biochemical measurements, with significance tested using paired t-tests or Wilcoxon tests. Covariance analysis (ANCOVA) will be used to adjust for confounding variables.

Participants needed: 40
Trial details
Age: 10-18Biological sex: AllType: InterventionalSponsor: Coordinación de Investigación en Salud, MexicoUpdated: Mar 24, 2025Locations: 1
Eligibility criteria

Male and female participants. [+4]

Patients with comorbidities not attributable to obesity, such as chronic kidney... [+4]

Status: Recruiting

Virtual Reality Versus Constraint-induced Movement on Hemiparesis in Cerebrovascular Event

The objective of this clinical trial is to measure the effect of Rehabilitation with Virtual Reality or Modified Constraint-Induced Movement Therapy on hemiparesis in patients with Cerebral Vascular Event. The question to be answered is: What is the effect of different therapeutic modalities supported by Virtual Reality or Modified Constraint-Induced Movement Therapy compared with usual Physical and Occupational Therapy on motor recovery of paretic limbs in patients with Cerebrovascular Event? The patients will carry out activities of: * Virtual reality or * Movement Restriction-Induction Therapy. The investigators will compare the changes in the functionality of the paretic hemibody with a group undergoing regular physical and occupational therapy, as well as language and treatment-related satisfaction.

Participants needed: 119
Trial details
Age: 35-70Biological sex: AllType: InterventionalSponsor: Coordinación de Investigación en Salud, MexicoUpdated: Aug 23, 2024Locations: 1
Eligibility criteria

Adult patients between 35 and 70 years of age and with a clinically and tomograp... [+7]

Patients who develop dementia or neurological-psychomotor complications during t... [+3]