To evaluate the Safety and efficacy of two Unani formulations in the treatment of overactive bladder.
Phase 2
- Conditions
- Health Condition 1: N329- Bladder disorder, unspecifiedHealth Condition 2: null- Zof-e-Masana (Overactive Bladder)
- Registration Number
- CTRI/2013/12/004258
- Lead Sponsor
- Central Council for Research in Unani Medicine CCRUM New Delhi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 300
Inclusion Criteria
1.Age- more than 18 yrs and upto 65 yrs
2.Gender- both
3.History of the following symptoms for more than six months
•Urgency of urine
•Incontinence
•Dysuria
Exclusion Criteria
Patients with Bladder calculus
2.Patients withUrinary tract infections
3.Patients with Benign Prostrate Hypertrophy
4.Patients with Uterine prolapse
5.Patients with Rectocele/cystocele
6.Patients with Cystitis
7.Patients with Diabetes Mellitus
8.Patients with Hypertension
9.Pregnant and lactating females
10.Neoplasm
11.Patients with Hepatic/Cardiac diseases
12.Medications (anticholinergic, antidepressant, psychotropic, or alpha-blocker)
13.Patients with History of any Spinal cord injury
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method