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Effect of curcumin addition to standard treatment on inflammation in endometrial carcinoma

Effect of curcumin addition to standard treatment on tumour-induced inflammation in endometrial carcinoma - Curcumun-2013

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2013-001737-40-BE
Enrollment
10
Registered
2013-06-04
Start date
2013-08-12
Completion date
Unknown
Last updated
2024-06-10

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

Conditions

endometrial carcinoma

Interventions

Product Code: Meriva Pharmaceutical Form: Tablet INN or Proposed INN: Curcuma Longa Extract CAS Number: 84775-52-0 Other descriptive name: CURCUMIN E100 Concentration unit: % (W/W) percent weight/weig

Sponsors

UZ Leuven
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Endometrial carcinoma, histologically confirmed No life-threatening metastases Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 5 F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range 5

Exclusion criteria

Exclusion criteria: Other active malignancy Documented autoimmune disease Currently ongoing immunosuppressive therapy Simultaneous treatment according to other clinical trials Documented immune deficiency

Design outcomes

Primary

MeasureTime frame
Main Objective: Evaluation of inflammatory markers in blood at regular time points Toxicity;Secondary Objective: Time to development of new metastases Response rate ;Primary end point(s): Effect on inflammatory mediators in blood;Timepoint(s) of evaluation of this end point: day 0, day 1, day 7, day 14, day 21

Secondary

MeasureTime frame
Secondary end point(s): Clinical response;Timepoint(s) of evaluation of this end point: baseline and after standard of care treatment

Countries

Belgium

Contacts

Public ContactClinical Trial Information

UZ Leuven

sandra.tuyaerts@uzleuven.be3216342905

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Mar 4, 2026