Clinical Trials Logo
  1. Home
  2. Uterine Cervical Dysplasia
  3. NCT01035580

Trial on Safety and Pharmacokinetics of Intravaginal Curcumin

Uterine Cervical Dysplasia Clinical Trial

Official title:
Phase I Trial on Safety and Pharmacokinetics of Intravaginal Curcumin in Normal Female Subjects

Clinical Trial Summary

The main objective of this study is to determine the maximum tolerable dose and safety of intravaginal curcumin in a normal population of women (women with no evidence of cervical cytological abnormalities by pap testing).

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01035580
Study type Interventional
Source Emory University
Contact
Status Completed
Phase Phase 1
Start date January 2010
Completion date January 2012
View Details
See also
  Status Clinical Trial Phase
Completed NCT01505920 - Lidocaine Spray Compared With Submucosal Injection During LEEP: a Randomized Controlled Trial Phase 3
Completed NCT01014026 - Self-sampling and Human Papillomavirus (HPV)-Testing for Unscreened Women in Cervical Cancer Prevention Phase 3
Completed NCT00377845 - Cervix Cytological Screening - Comparison of Tampon Self-Test and the Routine Smear. Phase 0
Completed NCT02910388 - LLETZ Under Direct Colposcopic Vision N/A
Completed NCT00596258 - A Two-Stage Phase 2 Study Of A-007 Topical Gel in High-Grade Squamous Intraepithelial Lesions (HSIL) Phase 2
Completed NCT03763565 - Effectiveness of HPV Vaccine in Thai Adult Women
Completed NCT04415840 - Lugol's Solution in Addition to Acetic Acid During Colposcopy
Recruiting NCT04783805 - Conservative Management of HSIL in Patients With Future Pregnancy Aspiration
Completed NCT04326049 - LLETZ With Videocolposcopy Versus LLETZ With Binocular Colposcopy N/A
Completed NCT02515162 - Fischer Cone Biopsy Excisor Versus Loop Excision Procedure for Conization N/A
Completed NCT02486471 - Hemostatic Procedure After Biopsy of the Cervix N/A
Completed NCT01405768 - Buffered Lidocaine for Loop Electrosurgical Excision Procedures (LEEPs) Phase 2
Completed NCT00264732 - A Study of Amolimogene (ZYC101a) in Patients With High Grade Cervical Intraepithelial Lesions of the Uterine Cervix Phase 2/Phase 3
Completed NCT03296566 - The SAFE Study: Satisfaction and Adherence to Follow-Up With Colposcopy Exams N/A
Completed NCT02346227 - Impact of AV2 Antiviral Drug on the Treatment of HPV-associated Lesions of the Uterine Cervix Phase 3
Completed NCT02330471 - Forced Versus Spray Coagulation in Women Undergoing LLETZ-conization for Cervical Dysplasia: a Randomized Trial Phase 3
Completed NCT01639820 - Comparison of Pelvic Lymphadenectomy Versus Isolated Sentinel Lymph Node Biopsy Procedure for Early Stages of Cervical Cancers : a Multicenter Study With Evaluation of Medico-economic Impacts N/A
Completed NCT00285207 - Safety and Efficacy of A-007 Topical Gel in the Treatment of High-Grade Squamous Intraepithelial Lesions (HSIL) of the Cervix Phase 2
Recruiting NCT05225493 - HIV Indicator Diseases in Hospital and Primary Care
Completed NCT01034358 - Immune Response to the Human Papillomavirus Vaccine in Young Women With Inflammatory Bowel Disease Phase 4