Using Misoprostol to Prevent Cervical Cancer
Official title: Misoprostol to Optimizing Prevention of Cancer of the Cervix: A Double-Blind Randomized Controlled Trial
Run by University of Alabama at Birmingham · NCT06669533 · Data updated 2026-11-12
This study is testing if the medication Misoprostol can help prevent cervical cancer in women who are being screened for the disease.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 25 Years and up |
| Sex | Women only |
| Enrollment | 840 (estimated) |
| Sponsor | University of Alabama at Birmingham Academic / other |
| Locations | 1 site (Yaoundé, Center Region) |
| Status | Recruiting |
| Started | February 25, 2025 |
| Main results expected | November 4, 2027 |
| Study ends | November 11, 2028 |
| Registry record updated | November 5, 2026 |
| Trial ID | NCT06669533 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are non-pregnant women aged 25 years or older with a confirmed diagnosis of Type 3 transformation zone.
✕Probably not a fit
Patients with Type 1 or 2 transformation zones, those who are currently pregnant, or individuals with a history of hysterectomy or active cervicitis may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This clinical trial involves a double-blind randomized controlled approach with 420 non-pregnant women who are undergoing cervical cancer screening using visual inspection with acetic acid. Participants diagnosed with Type 3 transformation zone (TZ) will be randomly assigned to receive either Misoprostol or a placebo. The goal is to evaluate the effectiveness of Misoprostol in optimizing the prevention of cervical cancer in this population.
Why it matters
Potential benefit: If successful, this study could enhance cervical cancer prevention strategies, potentially reducing the incidence of the disease.
How similar studies have gone: Other studies have explored the use of Misoprostol in cervical cancer prevention, indicating potential for success, though this specific approach may be novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Diagnosis of Type 3 TZ confirmed on exam prior to randomization * Age 25 years or older Exclusion Criteria: * With Type 1 or 2 TZ prior to randomization * Currently pregnant * History of hysterectomy * Any cancerous lesions * Active cervicitis
Where it's running
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Cameroon Baptist Convention Health Core, EtougEbe Baptist Hospital Yaoundé
Yaoundé, Center Region, Cameroon Recruiting
Study contacts
- Principal investigator: Warner K Huh, MD — University of Alabama at Birmingham
- Study coordinator: Warner K Huh, MD
- Email: whuh@uabmc.edu
- Phone: 2059341555
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Moderately hypofractionated radiotherapy after hysterectomy for cervical cancer
This study tests whether a shorter, moderately intensified radiotherapy course after surgery is safe and effective for patients with cervical cancer.
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Ivonescimab with paclitaxel and cisplatin before type A hysterectomy for Stage IB2/IIA1 (2–4 cm) cervical cancer
This trial will test whether adding ivonescimab to paclitaxel and cisplatin before surgery helps women with 2–4 cm (Stage IB2 or IIA1) cervical cancer shrink tumors so they can have a less radical (type A) hysterectomy.
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3- vs 4-fraction high-dose-rate brachytherapy for cervical cancer
This will test whether a three-fraction high-dose-rate brachytherapy schedule works as well as the standard four-fraction schedule for adults with locally advanced cervical cancer.
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Neoadjuvant immunochemotherapy for locally advanced cervical cancer
This trial will test whether giving paclitaxel and carboplatin together with a PD‑1/PD‑L1 immune checkpoint inhibitor before definitive treatment helps shrink tumors in patients with locally advanced cervical cancer (FIGO IB3–IIB) with tumors larger than 4 cm.
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IDOV-Immune for advanced solid tumors
This trial will try a single IV infusion of an engineered oncolytic vaccinia virus called IDOV-Immune in adults with advanced solid tumors that no longer respond to standard treatments.
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Combination of Iparomlimab and Tuvonralimab with Chemotherapy for Cervical Cancer
This study is testing whether combining two new immune treatments with standard chemotherapy can help women with locally advanced cervical cancer respond better to treatment before surgery.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.