Skip to content

Clinical trial on efficacy of dashmoola kwatha with goghrita in normal purperium

Randomized open controlled clinical trial to evaluate the add on effect of dashmoola kwatha with gou ghrita in Sutika awastha w.s.r. to normal purperium

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/06/043498
Enrollment
100
Registered
2022-06-27
Start date
Unknown
Completion date
Unknown
Last updated
2022-08-02

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

Conditions

Health Condition 1: Z392- Encounter for routine postpartum follow-up Health Condition 2: O868- Other specified puerperal infections

Interventions

None listed

Sponsors

Dr Radhika Amar Patil
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Purperial women irrespective of caste,parity,income group & occupation will be selected 2) Full term Normal Delivery cases will be selected 3) Cases without severe complications, PPH will be selected

Exclusion criteria

Exclusion criteria: 1)Women undergone ceaserean section 2)Women with Preterm Labour 3) Purperial Hypertension & Gestational Hypertension, GDM 4) Pre eclamptic Toxemia & gross anemia

Design outcomes

Primary

MeasureTime frame
To establish efficacy of dashmoola kwatha with goughrita in sutika paricharya WSR purperiumTimepoint: 6 weeks

Secondary

MeasureTime frame
1.To establish the efficacy of dashmoola kwatha with goughrita& its implication in routine post natal care 2.to support health status of mother during purpureal period 3.To prevent post-partum complications. 4.To study in details of sutika awastha & the changes which occur during this period by both ayurvedic & allopathic view. 5.To achieve restoration of dhatus to normal prepregnant state, Achieve good lactation & ensure well beingTimepoint: 6 weeks

Countries

India

Contacts

Public ContactDr Radhika Amar Patil

Yashwant Ayurved College Kodoli

kvt126@gmail.com9423277612

Outcome results

None listed

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