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Efficacy and Safety of Tirzepatide (Spartina) in Chronic Kidney Failure
Plain-language guide to NCT07176663: not phased interventional trial of Tirzepatide, 15 participants. Who took part, design and what was measured.
Key Facts
- Registry ID
- NCT07176663
- Phase
- not phased
- Status
- not yet recruiting
- Start
- 2026-02-01
- Completion (planned or actual)
- 2026-04-01
- Participants
- 15 (estimated)
- Design
- na, open label (everyone knows who gets what), treatment
- Conditions studied
- Obesity
- Results posted
- not yet
What This Study Did, in Plain Language
What Was Tested
This registered not phased trial tested Tirzepatide.
Diabetes management presents a complex clinical scenario marked by several challenges, especially in chronic kidney failure.
These include navigating potential drug interactions between oral antidiabetic therapies and other agents.
Furthermore, these patients may experience various adverse drug effects, such as lactic acidosis, electrolyte abnormalities such as hypomagnesemia, fluid retention, and lipid derangements, which can further augment overall morbidity.
It had 1 arm (groups): Spartina (experimental).
Weekly injection of Tirzepatide (Spartina).
The registry classes the interventions as drug.
More on the Plan
Investigators will conduct a single-center clinical trial at Labafinezhad Hospital in Tehran, Iran.
Inclusion criteria consisted of age ≥18 years and a history of chronic kidney failure with preexisting diabetes or obesity with a body mass index over 27. .
Major exclusion criteria included similar drug therapy for a duration of less than 3 months and nonadherence to tirzepatide therapy.
Who Took Part
15 planned participants were the target.
It was open to people of any sex aged from 18 years with no upper age limit.
Healthy volunteers were not accepted; participants needed the condition being studied.
How the Study Was Run
It was run as a single-group and open-label study.
Nothing was hidden in this open-label Tirzepatide study: the participants and staff both knew the treatment.
Everyone received the same intervention, so there was no separate comparison group inside the trial.
It started in 2026-02-01 with completion listed for 2026-04-01.
It ran at 1 site in Iran.
Its stated primary purpose is treatment.
What Was Measured
Primary outcome: weight loss (time frame: kilogram of weight loss measured by same scale one and three month after injection).
What This Means in Plain Language
Put simply, this is a not phased trial of Tirzepatide in 15 people.
Its size is small, so on its own it can only give an early look.
Its status is not yet recruiting; no results are posted to the registry yet, so nothing here describes outcomes.
More context: the Tirzepatide compound page, all human trials.
Our Notes on the Compound
Tirzepatide: A prescription peptide medicine that acts on both the GIP and GLP-1 receptors; Mounjaro and Zepbound contain the same active ingredient.
Related Pages
Source: ClinicalTrials.gov record. This explanation is written by PeptideWhiz from the public record. For research and education only. Not medical advice; no dosing information is given.