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A Randomised Clinical Study To Evaluate The Benefit of Adding An Ayurvedic Formulation(Garbhini Shoolhara Yoga) To Standard Treatment(Isoxsuprine hydrochloride) For Uterine Pain During Pregnancy

Randomised Controlled Clinical Trial To Study The Add On Effect Of Garbhini Shoolhara Yoga With Isoxsuprine hydrochloride In Garbhini Udarshoola W.S.R to Uterine Pain. - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/102875
Enrollment
60
Registered
2026-02-03
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Health Condition 1: O269- Pregnancy related conditions, unspecified

Interventions

None listed

Sponsors

Dr Prachi Subhash Prabhukhanolkar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Inclusion criteria Patient willing to give written consent for enrolment in study Pregnant women of any parity Gestational age between 12 and 34 weeks of live pregnancy Patient with intact amniotic membranes Pain in abdomen with mild uterine pain in pregnant women. Age from 18 to 40 years Cervical dilatation absent or having dilatation less than 2 cm. Cervical effacement absent or effacement should be less than 10%

Exclusion criteria

Exclusion criteria: Exclusion criteria Patient not willing to give written consent for enrolment in study. Multiple pregnancy Pain in abdomen with moderate or severe uterine contraction Cervical length less 20 mm in trans-vaginal Ultrasonography. Pre-mature rupture of membranes Placenta praevia or abruption Patient with ectopic pregnancy Patient with incomplete abortion or per vaginal bleeding Patient with intra-uterine fetal death (IUFD) Pregnancy with cervical dilatation more than 2cm. Pregnancy with cervical effacement more than 10% Pregnancy with cervical incompetence Evidence of urinary tract infection Previous history of pre-term labour. Previous history of habitual abortion

Design outcomes

Primary

MeasureTime frame
Subjective criteria 1. Duration of uterine pain 2. Frequency of uterine pain Objective criteria intensity of uterine pain by Visual Analogue Scale (VAS)Timepoint: Subjective criteria 1. Duration of uterine pain 2. Frequency of uterine pain Objective criteria intensity of uterine pain by Visual Analogue Scale (VAS) Assesement will be done on 1st day(before treatment) and on 5th day(after treatment)

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDr Manoj Gaikwad

R. A. Podar Medical College (Ayu), Worli, Mumbai

drmanojvgaikwad@gmail.com9822752816

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026