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Fasudil hydrochloride in the treatment of gene-specific ovarian cancer patients

Fasudil hydrochloride in the treatment of gene-specific ovarian cancer patients

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061789
Enrollment
Unknown
Registered
2022-07-02
Start date
2022-08-01
Completion date
Unknown
Last updated
2023-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ovary cancer

Interventions

first group:Fasudil Hydrochloride Injection
second group:Standard chemotherapy agent and placebo

Sponsors

Tianjin Medical University General Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: A total of 80 patients with recurrent ovarian cancer after pd clatinum-basehemotherapy, and the patients were randomly divided into 2 groups, with 40 patients in each group, and the age, pathological type, ECOG fitness score, prior chemotherapy plan and FIGO stage at initial treatment of patients in the two groups were completely matched. The inclusion criteria are as follows: 1. identified by genetic testing as A/A genotype; 2. aged 18-75 years; 3. ECOG score 0-1; 4. expected survival >= 3 months.

Exclusion criteria

Exclusion criteria: 1. Patients with hypotension and bleeding, such as cerebral hemorrhage; 2. Intracranial hemorrhage may occur: patients with bleeding aneurysms that have not been adequately hemostatic during surgery; 3. With uncontrollable pleural effusion, pericardial effusion or peritoneal effusion that requires repeated drainage 4. Giant aneurysm (diameter >= 2.5cm), vertebro-basal aneurysm; 5. With severe heart disease; 6. Patients with severe diabetes; 7. People with a history of mental illness before onset; 8. have severe liver and kidney insufficiency; 9. Persons with severe disturbance of consciousness.

Design outcomes

Primary

MeasureTime frame
Number of treatment courses received;Overall survival;progression free survival;objective response rate;complete remission;partial remission;

Secondary

MeasureTime frame
blood pressure;heart rate;

Countries

China

Contacts

Public ContactYingmei Wang
wangyingmei1978@126.com+86 15202229229

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026