Effect of hingvadi churna in post delivery backache: A clinical study

A randomised controlled clinical trial to study the effect of hingvadi churna in katishula with special reference to sutika roga . - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/07/071531

Enrollment

Registered

2024-07-30

Start date

Unknown

Completion date

Unknown

Last updated

2024-08-19

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

Conditions

Health Condition 1: O909- Complication of the puerperium, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: The signs and the Symptoms of puerperal women after normal delivery Full-term normal delivery irrespective of parity and gravida Married women. Patients between 18 -35 years of age. Patient willing to give written consent

Exclusion criteria

Exclusion criteria: L.S.C.S. Previous operations Patients with known case of Spine disorders Patients with Any previous surgeries/ lumbar / abdominal surgery Patients unwilling to give informed written consent. Age group below 18 years and above 35 years. High-risk pregnancies associated with known case of PIH, Pre- Eclampsia, Eclampsia, PPH, CPD.

Design outcomes

Primary

Measure	Time frame
To assess the effect of hingvadi churna in katishula with special reference to sutika roga with the help of assessment criteria after 14 days of treatmentTimepoint: Reduction in signs and symptoms of katishula in sutika after 14 days of treatment	—

Secondary

Measure	Time frame
To study effectiveness of trial and control groupTimepoint: 18 months	—

Countries

India

Contacts

Public ContactDr Sameer S Gholap

SMBT Ayurved college and hospital

drsameer.gholap@gmail.com9820304881

Outcome results