NCT07191873RecruitingPhase 4
Tirzepatide in Idiopathic Intracranial Hypertension Trial
A Phase IV Placebo-controlled Single Center Trial for Tirzepatide in Idiopathic Intracranial Hypertension Trial (TIIHT)
Source: ClinicalTrials.gov · Last updated 15 Sept 2026
Brief summary (registry, in English)
This will be a randomized, double-blind, parallel, placebo-controlled trial of 60 participants. The primary analysis will be a statistical comparison of the estimates of the mean difference in the 12-month change in intracranial pressure (ICP) between participants assigned to the tirzepatide and Placebo arms in 1:1 randomization using the intention-to-treat (ITT) population. Hypothesis testing will be performed using analysis of covariance (ANCOVA), with the treatment indicator as the independent variable and the 12-month change in ICP as the dependent variable. Models will include baseline ICP as a covariate. This primary endpoint will use a significance level of 0.05 to declare significance.
- Status (registry)
- Recruiting
- Phase (registry)
- Phase 4
- Study type
- Interventional
- Enrollment
- 60 (estimated)
- First submitted
- 17 Sept 2025
- Start date
- 25 Aug 2026
- Primary completion date
- Aug 2027
- Lead sponsor
- Duke University
- Diseases
- High blood pressure
- NCT number
- NCT07191873
What you commit to
- Study type: Interventional · Phase 4
- Planned participants: 60
- From 25 Aug 2026 to the primary completion date, Aug 2027
- 1 site 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 design.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Previous bariatric surgery
- Prior intervention for high ICP including optic nerve sheath fenestration (ONSF), venous stenting and/or shunting
- Taking another GLP-1 agonist, another drug that can interfere with the GLP-1 agonist, or any other anti-obesity medication
- Taking another medication to lower ICP in IIH (if previously taking another medication for ICP must be off this medication for at least 30 days prior to enrollment)
- No change in headache medications in the past 60 days
Other illness
- History of pancreatitis, personal or family history of medullary thyroid carcinoma or multiple endocrine neoplasia type 2 (MEN2), history of gallbladder disease, ulcerative colitis, Crohn's disease, or history of hypersensitivity reaction in response to the drug
- Other disorders causing visual loss and/or anomalous optic nerve
- Venous sinus thrombosis on magnetic resonance venography (MRV)
- Uncontrolled hypertension (≥140mmHg/90 mmHg)
- Exposure to a drug, substance, or disorder that has been associated with elevation of intracranial pressure within 2 months of diagnosis such as lithium, vitamin A, various cyclines
- Type II diabetes
Lab values
- Anemia (hemoglobin \[Hgb\] ≤ 8.0g/dL)
- eGFR \< 30 ml/min/1.73m2
Other
- Pregnancy or planning a pregnancy in the next 12 months or currently breastfeeding
- Papilledema Frisen Grade III, IV or fulminant IIH
- Mean perimetric deviation ≤ -7 dB
- CSF contents outside of normal limits
- Diagnosed sleep apnea with continuous positive airway pressure (CPAP) use
Who the study is looking for
- Signs and symptoms of increased intracranial pressure:
- headaches, tinnitus, visual obscurations, papilledema;
- absence of localizing findings on neurological examination (except for VI nerve palsy);
- no secondary causes identified on imaging, e.g., hydrocephalus, space- occupying lesion;
- elevated lumbar puncture (LP) opening pressure (OP) ≥25 cm H2O in lateral decubitus position with legs extended (\>= (≥ 20cm H2O if one of the following is present: pulse synchronous tinnitus, abducens palsy, Frisen grade II papilledema, transverse venous sinus stenosis, partially empty sella or enlarged optic nerve sheath on magnetic resonance imaging (MRI);
- the patient is awake and alert.
- BMI ≥30 kg/m2
- Age 18-60 years of age
- Unilateral or bilateral papilledema
- Able to provide informed consent
- Women of child-bearing age must use birth control (non-oral contraceptive method or add a barrier method of contraception).
Age in the registry: 18 years to 60 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Duke University Medical Center Coordinator of this site? Confirm its status | Durham | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.