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

PHASE1/PHASE2CompletedINTERVENTIONAL
Timeline

Start Date

Not specified

Study Completion Date

April 30, 2009

Conditions
Anal Resting Pressure
Interventions
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."

Trial Locations (1)

Unknown

Dept of Gastroeneterology, Asaf Harofe Medical Center, Zrifin

All Listed Sponsors
lead

RDD Pharma Ltd

INDUSTRY

NCT00816205 - An Open Label Study to Examine the Effect of Coated Nifedipine Suppositories on Anal Pressure in Healthy Subjects | Biotech Hunter | Biotech Hunter