Status:
COMPLETED
An Open Label Study to Examine the Effect of Coated Nifedipine Suppository on Anal Fissure Pain and Healing in Human Subjects
Lead Sponsor:
RDD Pharma Ltd
Conditions:
Chronic Anal Fissure
Eligibility:
All Genders
18-65 years
Phase:
PHASE1
PHASE2
Brief Summary
This is an open label study. The study will consist of 1 treatment group: coated Nifedipine suppository containing 12 mg of Nifedipine, administered BID to subjects with chronic anal fissure.
Detailed Description
This is an open label study. The study will consist of 1 treatment group: coated Nifedipine suppository containing 12 mg of Nifedipine. Approximately 20 subjects will participate into this 8-week stud...
Eligibility Criteria
Inclusion
- Single anal fissure
- Signed written informed consent
- Male or female subjects 18 to 65 years of age
- Has chronic anal fissure defined as history of anal pain at least three days a week for 30 days duration or more
- Visible fibers of the internal sphincter were seen at the base of the fissure or if a sentinel pile was present
- VAS of \> 35 mm in screening visit
- If female, is nonlactating, has a negative urine pregnancy test result, and does not plan on becoming pregnant during the study, or not of childbearing potential (hysterectomy or tubal ligation at least 6 months prior to entry to the study or post-menopausal for 1 year); if of childbearing potential (including peri-menopausal women who have had a menstrual period within one year) must practice or be willing to continue to practice appropriate birth control (such as implants, injectables, oral contraceptives, some intrauterine contraceptive devices, sexual abstinence, tubal ligation, or a vasectomized partner) during the entire study duration.
Exclusion
- Known allergy to Nifedipine, polyethylene-glycol, propylene Glycol or silicone
- Fissure resulting from inflammatory bowel disease, venereal disease, perianal psoriasis, immunodeficiency syndrome
- Anal abscess
- Fixed anal stenosis
- Active or past history of cardiovascular or cerebrovascular disease including unstable angina, myocardial infarction, transient ischemic attacks/stroke, clinically significant arrhythmia, moderate to severe congestive heart failure, or cardiac valve abnormalities
- Type 1 diabetes mellitus
- Insulin treated type 2 diabetes mellitus
- History of Renal insufficiency
- History of Liver insufficiency
- Malignant disease within 5 years of screening
- Has uncontrolled hypertension (sitting blood pressure \<160/95 mmHg at screening)
- History of chronic gastrointestinal disease
- History of rectal surgery
- History of gastrointestinal surgery
- History of HIV, hepatitis B, hepatitis C
- In need of chronic use of medication, with the exception of birth control medications
- Currently uses medication for acute illness (other than medications for use of treatment/pain relief of anal fissure)
- Has used, in the last four weeks, drugs that may affect blood coagulation, such as Aspirin at a dose higher than 500 mg/day , Warfarin, Sintrom, Enoxaparin, Nadroparin, Heparin, Clopidogrel, Ticlopidine
- Is using drug that may affect rectal tone
- Calcium Channel Blocker such as:
- Nifedipine (Osmo-Adlat, Pressolat, Nifedipine -Teva, Nifedilong)
- Amlodipine (Amlow, Norvasc, Amlodipine-Teva)
- Lercadipine (Vasodip)
- Verapamil (Ikacor, Ikapress, Verapress)
- Felodipine (Penedil)
- Diltiazem (Adizem, Dilatam)
- Nitrate donors such as:
- Glyceryl Trinitrate (Deponit)
- Isosorbid dinitrate (Isoket, Isolong)
- Isosrbid mononitrate (Monocord, Monolong, Mononit)
- Nitroglycerine (Nitrocine, Nitroderm, Nitrolingual)
- Has upon physical examination a rectal deformation or signs of rectal disease such as bleeding hemorrhoids, fistula., infection or space occupying lesion
- Is an immediate family member of personnel directly affiliated with the study at the investigative site, or is personally directly affiliated with the study at the investigative site; or is employed by RDD Pharma Ltd
Key Trial Info
Start Date :
December 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
February 1 2011
Estimated Enrollment :
20 Patients enrolled
Trial Details
Trial ID
NCT00972907
Start Date
December 1 2009
End Date
February 1 2011
Last Update
February 16 2011
Active Locations (2)
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1
Sapir Medical Center
Kfar Saba, Israel
2
Macabi HMO
Tel Aviv, Israel