Use of chatrujat yavagu in normal puerperium

RANDOMIZED OPEN CONTROLLED CLINICAL STUDY TO EVALUATE THE ADD ON EFFECT OF CHATURJATA YAVAGU IN SUTIKA AWASTHA W.S.R. TO NORMAL PUERPERIUM. - Nil

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/11/077179

Enrollment

100

Registered

2024-11-21

Start date

Unknown

Completion date

Unknown

Last updated

2024-12-09

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

Conditions

Health Condition 1: - Health Condition 2: O908- Other complications of the puerperium, not elsewhere classified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1) puerperal women irrespective of cast , parity, income group and occupation. 2) normal vaginal delivery cases . 3) women with preterm labour. 4) puerperal hypertension and gestational hypertension, Gdm

Exclusion criteria

Exclusion criteria: Women undergone Caesarean section

Design outcomes

Primary

Measure	Time frame
Evaluate the efficacy of chaturjata YAVAGU and implication in routine post natalcare .Timepoint: To achieve the outcome in 7 day F/u 15 th day F/u 30 th day F/U 45 th day	—

Secondary

Measure	Time frame
To study the chaturjata YAVAGU in respect to pain involution of uterus, lactation and appetite. 2) support health status of mother during puerperal period 3) study details of awastha and the changes which occur during this period by both ayurvedic and allopathic view.Timepoint: To achieve the outcome of study in 7 days.	—

Countries

India

Contacts

Public ContactDr Kavita Chandrashekhar Mule

ingolemira40@gmail.com7020154901

Outcome results