A Clinical Study To Test The Healing Effect Of Darvyadighrita When Applied To Episiotomy Wounds After Childbirth

An Open Randomized Controlled Clinical Study To Evaluate The Vranaropak Effect Of Darvyadighrita Local Application On Vitapchedan With Special Reference To Episiotomy Wound. - NIL

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/05/087940

Enrollment

Registered

2025-05-30

Start date

Unknown

Completion date

Unknown

Last updated

2025-06-24

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

Conditions

Health Condition 1: O860- Infection of obstetric surgical wound

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Primiparous women with normal vaginal delivery with episiotomy Multiparous women with normal vaginal delivery with episiotomy 1st and 2nd degree perineal tear Age group 19 to 40years Patient irrespective of Religion Cast Socio economic status Occupation Laboratory investigations for inclusion criteria CBC BSLR HIV HBSAG VDRL Urine routine Patients with informed written consent prior to delivery

Exclusion criteria

Exclusion criteria: Women with Systemic disorders like Diabetes Mellitus Hypertension Pulmonary tuberculosis Patients having perineal hematoma or abscess Patients with serology positive for HIV VDRL HBsAg HCV Normal delivery with intrapartum complications like PPH Manual removal of placenta 3rd and 4th degree perineal tear Severe Anaemic patients less than 7gm per dl Hb

Design outcomes

Primary

Measure	Time frame
VranaropanTimepoint: 7 days	—

Secondary

Measure	Time frame
Vranavedana (Pain) Vranagandha (Foul smell) Vranashotha (Inflammation) Vranastrava (Discharge)Timepoint: 7 days	—

Countries

India

Contacts

Public ContactDr Sujata Shrikant Jagtap

APMS Ayurved Mahavidyalaya Sion

anjalisavade88@gmail.com9970167582

Outcome results