MANAGEMENT OF scanty menses WITH 2 oral decoctions

MANAGEMENT OF ARTAVA KSHAYA WITH TILASHELUKARVI KWATHA AND VENUPARVADI KWATHA: A COMPARATIVE CLINICAL STUDY

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2018/11/016250

Enrollment

Registered

2018-11-01

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: Venuparvadi kwatha: venu soya guda Dose- 40 ml BD (Kwatha will be prepared by 20 grams of kwatha churna) Control Intervention1: TILASHELUKARVI KWATHA: tila shelu karvi guda Dose- 40 m

Eligibility

Inclusion criteria

Inclusion criteria: patients having any two of following symptoms - Duration of flow less than 3 days Reduced quantity of flow (using less than 2 pads/day)Patients suffering from 2 consecutive cycle with Oligo/Hypomennorhoea

Exclusion criteria

Exclusion criteria: Pregnant women Patients suffering from any systemic diseases Patient having any organic pathology of uterus and adnexae Patients having physiological infrequent menstruation Lactating mother Woman taking OCPs Hb level less than 7 gm%

Design outcomes

Primary

Measure	Time frame
Improvement in subjective and objective parametersTimepoint: Improvement in subjective and objective parameters in 2 months	—

Secondary

Measure	Time frame
Relief in artava kshayaTimepoint: 2 months	—

Countries

India

Contacts

Public ContactLaxmi devi

National institute of Ayurveda

drlaxmigupta90@gmail.com7275199081

Outcome results

None listed

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