Trial on Safety and Pharmacokinetics of Intravaginal Curcumin
This study has been completed.
Information provided by (Responsible Party):
Lisa Flowers, Emory University
First received: December 17, 2009
Last updated: November 27, 2013
Last verified: November 2013
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).
Uterine Cervical Dysplasia
||Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
||Phase I Trial on Safety and Pharmacokinetics of Intravaginal Curcumin in Normal Female Subjects
Primary Outcome Measures:
- The primary endpoint is to reach the maximum selected dose (MSD) or maximum tolerated dose (MTD) of intravaginal curcumin among Pap test negative women without causing a dose-limiting toxicity. [ Time Frame: 14 days ] [ Designated as safety issue: Yes ]
| Study Start Date:
| Study Completion Date:
| Primary Completion Date:
||April 2011 (Final data collection date for primary outcome measure)
This was a 3 + 3 dose escalation trial starting at 500 mg of cur cumin capsules administered daily intravaginally for 14 days. The dose increased after safety was demonstrated in 3 subjects by 500 mg up to a max of 2000 mgs.
Curcumin 500 mg capsules will be inserted intravaginally once daily for 14 days for a maximum daily dosage of 2000 mg
all patients received the drug
Other Name: Sabinsa Curcumin Capsules
|Ages Eligible for Study:
||18 Years to 45 Years
|Genders Eligible for Study:
|Accepts Healthy Volunteers:
- Between the ages of 18-45 years of age at enrollment
- Currently using a reliable birth control method (oral contraceptive pills, DepoProvera or permanent sterilization)
- Able to provide written informed consent
- Provide male partner notification letter
- Have a Pap test negative pap (no cervical intraepithelial lesions) within 45 days prior to screening
- Have regular monthly menses (every 21-35 days) or amenorrhea due to hormonal contraceptive use
- Agree to undergo pelvic exam and colposcopy per protocol
- Able and willing to complete Study Diary
- Agree to wear condoms during all acts of vaginal intercourse or abstain from vaginal intercourse during the 14 days
- Agree to abstain from sexual intercourse for 48 hours prior to the enrollment visit
- Agree to insert curcumin gelatin capsules as required per protocol
- Agree to abstain from nonsteroidal anti-inflammatory drugs (NSAIDS) during the 14 days
- Agree to abstain from all products containing curcumin or food consumption of curcumin during the 14 days
- Agree to abstain from the following activities for at least 48 hours prior to enrollment through the Day 14 visit:insertion of objects into the vagina except for a penis, receiving oral or anal sex,using a diaphragm, cervical cap, female condom, or vaginal contraceptive ring,using vaginal products other than the study gelatin capsules, including douches, lubricants, spermicide or feminine hygiene products,participating in other vaginal cream or contraceptive studies
- Agree to testing for HIV status via enzyme immunoassay (EIA)/Western Blot
- Are post-menopausal
- Have had a hysterectomy with removal of the cervix
- Have a clinically significant chronic medical condition that is considered progressive, including: coronary disease, congestive heart failure, chronic obstructive lung disease, diabetes mellitus, chronic renal disease, active peptic ulcer disease, chronic hepatic disease, multiple sclerosis, seizure disorder requiring medication, and a coagulation or platelet disorder. Chronic nonprogressive or intermittent syndromes are not excluded, including migraine headaches, mild reactive airways disease, controlled hypertension, stable pain syndromes, or benign gastric reflux.
- Have an intrauterine device (IUD) as a form of birth control
- Have any history of malignancy or current (within 45 days of screening) pap with cervical intraepithelial lesions.
- Currently has documented lacerations on visual inspection present on the cervix, vagina, vulva or perineum.
- Are pregnant or planning to become pregnant in the next three months
- Are currently breastfeeding
- Have a history of sensitivity or allergy to any compound used in this study
- Have Grade 2 or higher renal or hematologic abnormality, as defined by the Table for Grading the Severity of Adult Adverse Events or at screening have a positive bacterial urine culture. Women with a positive bacterial urine culture at screening will be allowed to enroll after appropriate treatment if repeat evaluation is normal.
- In the three months prior to enrollment have had any of the following:Treatment for Cervical disease or any other gynecologic surgery,A pregnancy or an abortion, An IUD,Breakthrough menstrual bleeding or vaginal bleeding during or following vaginal intercourse
- Signs, as seen on pelvic exam at screening, consistent with an STD including vaginitis, cervicitis or genital ulcers
- Signs, as seen on pelvic exam, of genital trauma
- Signs of genital tract infection from laboratory evaluations. Women with Candida vaginitis or bacterial vaginosis at screening will be allowed to enroll after appropriate treatment and if repeat evaluation is normal.
- In the three months prior to enrollment have had any of the following:History of treatment for or a diagnosis with a new STD,Genital herpes simplex virus infection or outbreak,Exchanged sex for money, drugs or gifts
- Are currently using, or in the last year have used intravenous drugs (except for therapeutic use), cocaine or other recreational drugs, abused alcohol defined as alcohol use that has required hospital admission for detoxification and therapy.
- Have any other condition that in the opinion of the investigator might interfere with the evaluation of the study objectives.
- HIV positive
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study.
To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below.
For general information, see Learn About Clinical Studies.
Please refer to this study by its ClinicalTrials.gov identifier: NCT01035580
|Atlanta, Georgia, United States, 30303 |
||Lisa Flowers, Medical
No publications provided
||Lisa Flowers, Principal Investigator, Emory University
History of Changes
|Other Study ID Numbers:
|Study First Received:
||December 17, 2009
||November 27, 2013
||United States: Food and Drug Administration
Keywords provided by Emory University:
Additional relevant MeSH terms:
ClinicalTrials.gov processed this record on March 01, 2015
Uterine Cervical Dysplasia
Genital Diseases, Female
Uterine Cervical Diseases
Anti-Inflammatory Agents, Non-Steroidal
Central Nervous System Agents
Molecular Mechanisms of Pharmacological Action
Peripheral Nervous System Agents
Physiological Effects of Drugs
Sensory System Agents