Randomized controlled clinical trial to evaluate the role of aaragwadha patra taila in garbhini kikwisa w.s.r.to striae gravidarum
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 80
- Locations
- 1
- Primary Endpoint
- 1.Kandu (Itching)
Study Overview
Brief Summary
Kikwisa is seen in 70 -90 %11 of all Garbhini patients attending in
Streeroga and Prasutitantra OPD. It is the major problem of modern
cosmatic conscious era. So, it requires medical treatment which is cost
effective and with less side effects .
Aaragwadha patra Kalka is mention in Vaidya Manorama and
Karveerpatra siddha taila is mention in Charaka samhita and Asthang
Hridaya for the management
of Garbhini kikwisa. By taking these drugs I
am going to prepare Taila which is easy to apply and it is cost effective
and all drugs to be used in it are easily available.
So, present study is to evaluate the role of Aaragwadha patra taila in
Garbhini kikwisa being proposed.
Study Design
- Study Type
- Interventional
- Allocation
- Coin toss, Lottery, toss of dice, shuffling cards etc
- Masking
- None
Eligibility Criteria
- Ages
- 18.00 Year(s) to 30.00 Year(s) (—)
- Sex
- Female
Inclusion Criteria
- •i)Patients willingly participating in the trial and giving consent form.
- •ii)Primi gravidae patients will be selected for study.
- •iii) Patients with gestational age of 7 th month onward up to delivery.
- •Iv) Patients having classical sign and symptoms of Garbhini kikwisa as per prepared Performa will be selected.
Exclusion Criteria
- •i)Multi-gravida ii) Diabetic mother.
- •iii) Patients not willing to participate in the trial.
- •iv) Any malignancy on the affected part v) Patients having skin disease.
Outcomes
Primary Outcomes
1.Kandu (Itching)
Time Frame: First day,30th day,60th day,90th day,120th day
2.Vidaha (Burning sensation)
Time Frame: First day,30th day,60th day,90th day,120th day
3.Vali vishesh (Strech mark)
Time Frame: First day,30th day,60th day,90th day,120th day
4.Vaivarnyata (Discolouration)
Time Frame: First day,30th day,60th day,90th day,120th day
all symptoms will be decreased
Time Frame: First day,30th day,60th day,90th day,120th day
Secondary Outcomes
- Above all symptoms will be decreased(4 months)
Investigators
Dr Shital Dnyanoba More
Matoshree Asarabai Darade Ayurved College Babhulgoan ,Yeola