An Open Label Study to Examine the Effect of Coated Nifedipine Suppositories on Anal Pressure in Healthy Subjects

Anal Resting Pressure Clinical Trial

Official title:

An Open Label Study to Examine the Effect of Coated Nifedipine Suppositories on Anal Pressure in Healthy Subjects

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00816205
• Other study ID #: RDD102
• Status: Completed
• Phase: Phase 1/Phase 2
• First received: December 31, 2008
• Last updated: April 6, 2009
• Est. completion date: April 2009

Study information

• Verified date: April 2009
• Source: RDD Pharma Ltd
• Contact: n/a
• Is FDA regulated: No
• Health authority: Israel: Ministry of Health
• Study type: Interventional

Clinical Trial Summary

This is an open label, dose-finding study. Approximately 8 healthy subjects will be participating in this study.

Within one week after the screening visit, subjects who meet all inclusion criteria and none of the exclusion criteria will enter a one day treatment period. During this period, 4 anal manometric studies will take place. Study medication (Coated Nifedipine suppositories at various doses) will be administered at pre-determined intervals. During the study, blood samples will be obtained for plasma Nifedipine analysis.

Description:

After detrminig baseline resting anal pressure with a manometric test, coated Suppositories will be administered intra rectally. Subjects will take rectally a total of 3 Coated Suppositories per study. 90 minutes after each coated suppository insertion this suppository will be removed and a amnometric study will be performed:

The first dose will contain 4 mg of Nifedipine and the manomentric measurement performed afterwards will be used to determine baseline anal pressures.

The second dose will contain 12 mg of Nifedipine. The third dose will contain 24 mg of Nifedipine. The primary efficacy parameter is change in Resting Anal Pressure from baseline.

The secondary efficacy parameters include the following:

• The ratio of change in anal pressure to plasma Nifedipine level.

• The ratio of change in anal pressure to change in blood pressure.

• The ratio of change in anal pressure to change in heart rate.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 0
• Est. completion date: April 2009
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

Subjects meeting the following criteria will be eligible to participate in the trial:

• Signed written informed consent;

• Male or female subjects 18 to 55 years of age;

Exclusion Criteria:

Subjects are excluded from participation in the study if any of the following criteria apply:

Has a clinically significant history or presence of any of the following conditions:

• Known allergy to Nifedipine, polyethylene-glycol, Propylene-glycol or silicone.

• Active or past history of disease that requires medication or clinical follow up.

• Malignant disease within 5 years of screening;

• History of ano rectal disease.

• History of gastrointestinal disease.

• History of gastrointestinal bleeding.

• History of rectal surgery.

• History of gastrointestinal surgery.

• History of HIV.

• In need of chronic use of medication, with the exception of birth control medications.

• Currently uses medication for acute illness.

• Has upon physical examination a rectal deformation or signs of rectal disease such as fissure, bleeding hemorrhoids, fistula., infection or space occupying lesion.

• Has received any investigational drug within 90 days of screening;

• Receipt of any investigational treatment (drug or device) within 90 days prior to screening;

Study Design

Intervention Model: Single Group Assignment

Related Conditions & MeSH terms

• Anal Resting Pressure

Intervention

Drug:
• Coated Nifedipine Suppositories
Subjects will take rectally a total of 3 Coated Suppositories per study. 90 minutes after each coated suppository insertion this suppository will be removed and a amnometric study will be performed: The first dose will contain 4 mg of Nifedipine and the manomentric measurement performed afterwards will be used to determine baseline anal pressures. The second dose will contain 12 mg of Nifedipine. The third dose will contain 24 mg of Nifedipine.

Locations

Country	Name	City	State
Israel	Dept of Gastroeneterology, Asaf Harofe Medical Center	Zrifin

Sponsors (1)

Lead Sponsor	Collaborator
RDD Pharma Ltd

Country where clinical trial is conducted

Israel, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The primary efficacy parameter is change in Resting Anal Pressure from baseline.		1 day	No