Randomized clinical control trial on efficacy of shatpushpa taila in vitapched janya vrana seevan karma pradesh with special reference to episiotomy wound

Randomized clinical control trial on efficacy of Shatpushpa taila in vitapched janya vrana seevan karma pradesh  with special reference to episiotomy wound

Primary objective

To study the efficacy of Shatpushpa  taila in vitapched janya vrana seevan karma pradesh wsr episiotomy wound

Secondary objective

To study the literature regarding episiotomy

To study properties of Shatpushpa

To study the efficacy of Shatpushpa tail against povidone iodine ointment

Patients will be divided in two groups

Group A and Group B and will be given Shatpushpa taila local application and povidone iodine ointment local application respectively

for 15 days

Clinical assessment will be done on day 1 day 3 day 7 day 14 day 21

Inclusion criteria

age 20 to 35 years

Patient who has undergone episiotomy procedure of any parity will be selected

Exclusion criteria

Perineal tear

Patient having blood coagulopathy

Prolonged labor PPH

Patient suffering from Diabetes mellitus Hypertension etc

VDRL HBSaG positive patients

Patients having history of episiotomy complications in previous delivery example Keloid Gap Resuturing

Withdrawal criteria

Occurence of serious adverse event of any cause

If patient want to withdraw her from this experiment

If patient absent for follow up will be considered as dropped from this project

Primary outcome

Presence of signs of healing of episiotomy wound in 7 days of start of treatment

Secondary outcome

Complete healing of episiotomy wound in 21 days of start of treatment

All data will be collected from clinical case studies will be presented in the form of graph charts healing grade

Patients will be observed before and after treatment

All observed data collected after the final assessment will be subjected to statistical analysis