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NCT06942377Not yet recruitingPhase 2

Calcium Channel Blocker Amlodipine for Endometrial Cancer Therapy

Peking University People's Hospital

Source: ClinicalTrials.gov · Last updated 8 Jul 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

To explore the treatment efficacy of Progesterone Therapeutic Regimen Plus Amlodipine in patients with early endometrial carcinoma (EEC) for conservative treatment.

Status (registry)
Not yet recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
140 (estimated)
First submitted
10 Mar 2025
Start date
15 Jul 2025
Primary completion date
1 Jan 2027
Lead sponsor
Peking University People's Hospital
NCT number
NCT06942377

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 140
  • From 15 Jul 2025 to the primary completion date, 1 Jan 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, 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

  • Individuals with contraindications to conservative treatment or medication use
  • Patients who have taken other types of antihypertensive drugs regularly in the past

Other illness

  • Merge malignant tumors from other parts

Other

  • Tumor invasion of muscle layer\>1/2, FIGO (2009) stage IB or above
  • Tumor differentiation into G3 or non endometrioid adenocarcinoma
  • Patients known to have experienced hypotension

Who the study is looking for

  • Pathological diagnosis of endometrial adenocarcinoma G1-2 of the endometrium
  • If the pathology is endometrial cancer, MRI or ultrasound confirms that the lesion is limited to the endometrium or invading the muscle\<1/2, that is, FIGO (2009) stage IA
  • Age ≤ 45 years old
  • Require those who wish to retain their reproductive function to sign informed consent
  • No serious internal medicine complications (severe liver and kidney dysfunction)
  • No contraindications for progesterone treatment or pregnancy
  • Has not experienced hypotension more than three times in the past six months and can be regularly monitored for blood pressure
  • Imaging shows no evidence of distant metastasis
  • A. Initial treatment patients: have not used any protective treatment drugs (progestogens, GNRH-a); B. One course of treatment (12 weeks) with incomplete remission of the lesion (partial remission, persistent or progressive lesion); C. Two courses of treatment (24 weeks) with incomplete remission (partial remission, persistent or progressive lesions);

Age in the registry: 18 years to 45 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
Peking University People's Hospital
Coordinator of this site? Confirm its status
BeijingChinaUnknown status

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