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A clinical trial on Ayurvdic therepy in delayed and scanty menses

A Randomized open label comparative clinical study of Shatapushpa Kalpa with Shatapushpa taila matra basti and Tilashelukaravi kwatha in the management of Artava Kshaya

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/04/024739
Enrollment
30
Registered
2020-04-20
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: N915- Oligomenorrhea, unspecified

Interventions

Intervention1: Shatapushpa Kalpa and Shatapushpa taila: Dose of Shatapushpa kalpa- on first day of menses starting with 6 gm of Shatapushpa churna with Ghrita , by gradually increasing 1gm./day and co

Sponsors

National Institute of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age- 15-40 years, Married/ Unmarried patients having any of following symptoms :- 1. Patient willing and able to participate in the study with written informed consent. Consent will be taken from guardian of those patient below 18 years of age. 2. Duration of flow less than 3 days with reduced quantity of flow (using less than 2 pads/day) with or without pain. 3. Interval between 2 cycles exceeding more than 35 days with or without pain. 4. Patients suffering from 2 consecutive cycles of Oligomenorrhoea and or Hypomennorhoea both.

Exclusion criteria

Exclusion criteria: 1. Patients having physiological infrequent menstruation. 2. Pregnant women. 3. Lactating mothers 4. Women taking OCPs. 5. Patients suffering from any systemic diseases. 6. Patients having any organic pathology of uterus and adnexa. 7. Hb. level less than 7 gm%.

Design outcomes

Primary

MeasureTime frame
To regularize menstrual cycle with normal flow of menstrual bleeding. Timepoint: after 8 weeks

Secondary

MeasureTime frame
Relief in associated features like painful menstruation etc.Timepoint: after 8 weeks.

Countries

India

Contacts

Public ContactDr Hetal H Dave

National Institute of Ayurveda

hetaldave2406@gmail.com9251758867

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026