A clinical study to assess the effect of Vamshapatra kwatha in women having delayed and scanty menstrual periods

A Randomized Controlled Clinical Study to evaluate the efficacy of Vamshapatra Kwatha in Artavakshaya - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/12/099695

Enrollment

Registered

2025-12-23

Start date

Unknown

Completion date

Unknown

Last updated

2026-01-12

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

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Women aged between 16 to 35 years Patients with history of artavakshaya in atleast 2 previous cycle Yathochitakala adarshanam of artava the interval between 2 cycles exceeds more than 35 days Haemoglobin greater than 11 gm per dl

Exclusion criteria

Exclusion criteria: Patients suffering from any systemic diseases Pregnant woman and lactating mother Known case of HIV and HBsAg positive Endometrial or cervical or breast carcinoma or any malignant diseases Thyroid disorders Female using oral contraceptives IUCD injectable contraceptives Any congenital anomalies

Design outcomes

Primary

Measure	Time frame
Interval between the cycles and duration of bleeding and amount of bleedingTimepoint: Interval between the cycles and duration of bleeding and amount of bleeding assessed at baseline and after completion of treatment of 8 weeks and during the third menstrual cycle follow up without medication	—

Secondary

Measure	Time frame
Increase in amount of bleeding, cycle regularisationTimepoint: Assessed at baseline,4 weeks, 8 weeks	—

Countries

India

Contacts

Public ContactDr Kavya M Rao

Alvas Ayurveda Medical College

drsumaranirajesh@gmail.com9449664617

Outcome results