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NCT07262762Completed

Spartina® (Tirzepatide) Effectiveness and Safety Evaluation

A Post-marketing Real-world Study for Evaluating Effectiveness and Safety of Spartina® (Tirzepatide Manufactured by CinnaGen) in Patients With Obesity and Overweight

Source: ClinicalTrials.gov · Last updated 15 Jul 2026

Brief summary (registry, in English)

The goal of this study is to evaluate Effectiveness and safety of Spartina® (Tirzepatide) in male or female participants with obesity and overweight. The main questions which are aimed to be answered: 1. Is Spartina® (Tirzepatide) effective in the treatment of obesity and overweight? 2. Is Spartina® (Tirzepatide) safe in the treatment of obesity and overweight? In this study, there is no comparison group. Participants receive Spartina® (Tirzepatide)

Status (registry)
Completed
Study type
Observational
Enrollment
175 (actual)
First submitted
23 Nov 2025
Start date
11 Nov 2025
Primary completion date
20 Jun 2026
Lead sponsor
Cinnagen
Diseases
Obesity
NCT number
NCT07262762

What you commit to

  • Study type: Observational
  • Participants enrolled: 175
  • From 11 Nov 2025 to the primary completion date, 20 Jun 2026
  • 14 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior use of any GLP-1 agonist in the last 6 months

Other illness

  • Type 1 diabetes mellitus
  • Any condition or circumstance that might pose a risk to the subject or interfere with the ability to acquire satisfactory clinical data
  • Personal or family history of medullary thyroid carcinoma (MTC) or patients with multiple endocrine neoplasia syndrome type 2 (MEN 2)

Other

  • Pregnancy or breast-feeding

Who the study is looking for

  • Male or female ≥18 years of age
  • Willingness for signing and having signed the informed consent form
  • BMI ≥30 kg/m² or ≥27 kg/m² with ≥1 weight-related comorbidity

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (14)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hajieh Bibi Shahbazian Clinic
Coordinator of this site? Confirm its status
AhvāzIranUnknown status
Mansoor Siavash Dastjerdi Clinic
Coordinator of this site? Confirm its status
IsfahanIranUnknown status
Shokoofeh Bonakdaran Clininc
Coordinator of this site? Confirm its status
MashhadIranUnknown status
Behrang Motamed Clinic
Coordinator of this site? Confirm its status
RashtIranUnknown status
Seyed Mojtaba Mehrdad Clinic
Coordinator of this site? Confirm its status
RashtIranUnknown status
Sari Diabetes Research Center
Coordinator of this site? Confirm its status
SariIranUnknown status
Dr. Mohammadhossein Dabbaghmanesh Clinic
Coordinator of this site? Confirm its status
ShirazIranUnknown status
Akbar Aliasgarzadeh Clinic
Coordinator of this site? Confirm its status
TabrizIranUnknown status
Alireza Esteghamati clinic
Coordinator of this site? Confirm its status
TehranIranUnknown status
Iran University Endocrinology Research Center
Coordinator of this site? Confirm its status
TehranIranUnknown status
Mohammadreza Mohajeri Tehrani Clininc
Coordinator of this site? Confirm its status
TehranIranUnknown status
Farzad Hadaegh Clininc
Coordinator of this site? Confirm its status
TehranIranUnknown status
Imam Khomeini Hospital
Coordinator of this site? Confirm its status
TehranIranUnknown status
Khorshid Clinic
Coordinator of this site? Confirm its status
YazdIranUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.