Safety and Effectiveness of Tirzepatide in Patients With Obesity at Hospital de Clínicas, Paraguay

LABORATORIOS INDUFAR

Status: Not yet enrolling

Conditions: Overweight With Comorbidities; Type 2 Diabetes Mellitus; Obesity

Treatments: Drug: Tirzepatide (T.G.)

Study type: Observational

Funder types: Industry

Identifiers

NCT07492563

TG-PY-001

Details and patient eligibility

About

This is a Phase 4 observational study evaluating the safety and effectiveness of tirzepatide (T.G.) manufactured by INDUFAR S.A. in 300 patients with obesity treated at the Obesity Unit of Hospital de Clínicas in Paraguay over 12 months. The primary objective is to assess the safety profile through monitoring adverse events. Secondary objectives include evaluating weight loss, metabolic parameters improvement, and treatment satisfaction in real-world clinical practice.

Full description

This prospective, single-center, open-label, observational Phase 4 study will enroll 300 patients with obesity (BMI ≥27 kg/m² with comorbidities or BMI ≥35 kg/m²) with or without type 2 diabetes at the Obesity Unit of Hospital de Clínicas, Asunción, Paraguay.

Patients will receive tirzepatide subcutaneously once weekly following a dose-escalation schedule: 2.5 mg (weeks 1-4), 5 mg (weeks 5-8), with optional escalation to 7.5 mg, 10 mg, 12.5 mg, or 15 mg based on tolerability and response. The medication will be provided free of cost by the sponsor INDUFAR S.A.

The study includes 4 in-person visits (baseline, months 3, 6, 12) and 2 telephone contacts (months 1, 9). Assessments include physical examination, laboratory tests (HbA1c in diabetics, fasting glucose, lipid profile, renal and hepatic function), adverse event monitoring, and quality of life questionnaires.

Primary endpoint: Incidence, type, severity, and outcome of adverse events during 12 months, with special attention to serious adverse events and events of special interest (pancreatitis, severe hypersensitivity, severe hypoglycemia, biliary disease, acute kidney injury).

Secondary endpoints: Change in body weight and BMI, proportion achieving ≥5%, ≥10%, ≥15% weight loss, change in HbA1c (in diabetics), cardiometabolic parameters, treatment adherence, and patient satisfaction.

This study will generate the first evidence on tirzepatide in the Paraguayan population and support clinical decision-making regarding use of this dual GIP/GLP-1 receptor agonist in real-world obesity management.

Enrollment: 300 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age ≥18 years
• BMI ≥27 kg/m² with weight-related comorbidities OR BMI ≥35 kg/m²
• Clinical indication for tirzepatide per treating physician
• Paraguayan citizenship or permanent residence
• Residence in Asunción or Metropolitan Area or possibility to assist to regular visits
• Ability to attend visits for 12 months
• Ability to provide written informed consent

Exclusion criteria

• Type 1 diabetes or secondary diabetes
• Known hypersensitivity to tirzepatide
• Personal or family history of medullary thyroid carcinoma or MEN 2 syndrome
• Acute pancreatitis in last 12 months or chronic pancreatitis
• Severe gastrointestinal disease
• Bariatric surgery in last 12 months
• Pregnancy or breastfeeding
• Severe renal impairment (eGFR <30 mL/min/1.73m²)
• Severe hepatic impairment (Child-Pugh B or C)
• Unstable cardiovascular disease
• Active cancer (except non-melanoma skin cancer completely resected)
• Current use of other GLP-1 receptor agonists
• Participation in another interventional trial within 30 days

Trial design

300 participants in 1 patient group

Tirzepatide Treatment Group

Description:

All enrolled patients receiving tirzepatide according to clinical indication

Treatment:

Drug: Tirzepatide (T.G.)