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Exploring the impact of nutritional interventions on clinical prognostic outcomes in patients with intermediate and advanced ovarian cancer undergoing primary debulking surgery

Exploring the impact of nutritional interventions on clinical prognostic outcomes in patients with intermediate and advanced ovarian cancer undergoing primary debulking surgery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097773
Enrollment
Unknown
Registered
2025-02-25
Start date
2025-03-20
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Ovarian cancer

Interventions

Intervention grop:Impact@ immunonutrition intervention

Sponsors

Zhejiang Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. aged over 18 years and under 75 years; 2. patients diagnosed with ovarian cancer confirmed by histological or cytological diagnosis, who are intended to be treated by primary debulking surgery; 3. with NRS-2002 score >= 3, ECOG score 35.0 g/L or albumin < 30 g/L but can be increased to 35.0 g/L after 7-14 days of nutritional intervention with isolated whey protein components; 4. lifetime expectancy greater than 6 months; 5. can tolerate enteral and parenteral nutritional therapy; 6. patients are able to give informed consent, agree to participate in the study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. patients changing their programme to NACT; 2. patients who are not suitable for body composition analyses, e.g., those in whom the presence of metallic substances in the body, such as internal fixators, pacemakers, etc., may affect the results; 3. any sign of severe or uncontrolled systemic disease that, in the opinion of the investigator, may significantly affect the patient's risk/benefit balance, including uncontrolled hypertension, hepatitis B, hepatitis C, and human immunodeficiency virus; 4. preoperative albumin <35.0 g/L and remains below 35.0 g/L after 7-14 days of nutritional intervention with isolated whey protein components; 5. patients who had primary tumour at other sites within 3 years; 6. female patients who are pregnant or breast-feeding; 7. according to the investigator, patients who were not suitable for inclusion or had poor adherence to the study.

Design outcomes

Primary

MeasureTime frame
Post-operative complication rate within 30 days;

Secondary

MeasureTime frame
Length of hospitalisation;Rate of unplanned secondary operations;30-day unplanned re-admission rate;Time to first chemotherapy;Nutritional status of patients;

Countries

China

Contacts

Public Contacttao zhu; yi lu

Zhejiang Cancer Hospital

luyi@zjcc.org.cn+86 135 8831 6980

Outcome results

None listed

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