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Effect of Sitz bath of pods of babool in abnormal vaginal discharge

Effect of Abzan of Samar Babool in Sayalan al-Rahim- A randomized controlled study - -

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/02/012175
Enrollment
72
Registered
2018-02-27
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Abnormal vaginal discharge Health Condition 2: N768- Other specified inflammation of vagina and vulva

Interventions

Intervention1: orally placebo and locally Pods of Acacia arabica Willd: orally one capsule(250 mg) of placebo will be given daily for 10 days and locally Joshanda(Extract) will be made and Abzan (sitz

Sponsors

National Institute of Unani Medicine
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Married women within the age group of 18â??50 years. Women presenting with abnormal vaginal discharge and/or associated with any of these symptoms such as dyspareunia, dysuria, burning micturition, vulval itching and/or vaginal malodour etc.

Exclusion criteria

Exclusion criteria: Pregnant, lactating and unmarried women. Patients with any undiagnosed uterine or vaginal bleeding, ulceration, vaginal douches and genital malignancies. Patients with suspicion of or clinically manifested with venereal diseases.

Design outcomes

Primary

MeasureTime frame
Change in abnormal vaginal discharge and/or any associated symptoms assessed by VAS Modified McCormack pain scale abdominal pain and rebound tendernessTimepoint: 0, 11th, 30th, 45th day

Secondary

MeasureTime frame
Change in quality of life assessed by EQ-5D-5L questionnaire. Timepoint: 0, 11th, 30th, and 45th day;Treatment satisfication questionnaire for medicationTimepoint: on day 11

Countries

India

Contacts

Public ContactDr Arshiya Sultana

National Institute of Unani Medicine,

drarshiya@yahoo.com9740915911

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 12, 2026