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NCT07366242Not yet recruiting

Prognostic Value of (DHODH) Expression in (HGSOC): A Comparative Study Between Neoadjuvant and Adjuvant Chemotherapy Settings

Prognostic Value of Dihydroorotate Dehydrogenase (DHODH) Expression in High-Grade Serous Ovarian Carcinoma: A Comparative Study Between Neoadjuvant and Adjuvant Chemotherapy Settings

Source: ClinicalTrials.gov · Last updated 26 Jan 2026

Brief summary (registry, in English)

* To compare DHODH protein expression in HGSC tissues from patients undergoing Primary Debulking Surgery (PDS - Chemo-naive) versus Interval Debulking Surgery (IDS - Post-NACT). * To evaluate the association between DHODH expression and the degree of chemotherapy response (using the Chemotherapy Response Score - CRS for NACT cases). * To determine the prognostic value of DHODH expression in predicting Platinum-Free Interval (PFI) ,Progression -Free Survival (PFS) and Overall Survival (OS) across both groups.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
72 (estimated)
First submitted
10 Jan 2026
Start date
1 Jun 2026
Primary completion date
1 Jun 2027
Lead sponsor
Heba Ahmed Mohamed
NCT number
NCT07366242

What you commit to

  • Study type: Observational
  • Planned participants: 72
  • From 1 Jun 2026 to the primary completion date, 1 Jun 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.

Other

  • Non-serous histological subtypes
  • Low-grade serous carcinoma
  • Inadequate tissue for immunohistochemistry
  • Missing clinical or follow-up data

Who the study is looking for

  • Histologically confirmed high-grade serous ovarian carcinoma
  • Availability of adequate FFPE tumor tissue
  • Known treatment modality (PDS or IDS)
  • Available clinical follow-up including platinum-free interval and survival data

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
Assiut University
Coordinator of this site? Confirm its status
AsyutEgyptUnknown status

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