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A Clinical trial to study dawa-e-munqabiz and encirclage operation in patients with cervical incompetence

Comparative study of dawa-e-munqabiz and encirclage operation in patients with cervical incompetence Eg. A randomized comparative,single blind, single centre,clinical trial to compare unani formulation dawa-e-munqabiz and encirclage operation in patients with cervical incompetence - RCSB

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2016/01/006521
Enrollment
150
Registered
2016-01-14
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- OBSTETRICAL OUTCOME IN CERVICAL INCOMPETENCE,PREGNANCY

Interventions

Intervention1: STUDY GROUP-DAWA-E-MUNQABIZ ORAL-DARONICUM HOOKANI LINN,BAMBOO MANNA BAMBUSA,SHELL,ASOKA BARK AND INTERNALLY USED ARE PUNICA GRANATUM LINN,ROSE POLLEN ,HONEY GIVEN IN DOSE OF TWO GRAMS

Sponsors

Government nizamia tibbi college and general hospitalnear charminar hyderabad
Lead Sponsor
Dr NTR UNIVERSITY OF HEALTH SCIENCES VIJAYWADA
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: The inclusion criteria includes women with two or more pregnancies, H/o previous spontaneous mid trimester abortions, H/o encirclage operations in previous pregnancies, USG findings with cervical dilatation of internal os, shortening of cervix, funnelling, cervical length less than 25mm. Cervical stitch criteria includes the women with cervical incompetence in the gestational period of12-18 weeks.

Exclusion criteria

Exclusion criteria: Exclusion criteria includes uterine development defects, uterine anomalies, foetal abnormalities, fulminant pre-eclampsia with BP >160/110mmHg, Abruption placenta, placenta Previa and polyhydramnios

Design outcomes

Primary

MeasureTime frame
Mean beck depression score is ten calculated in percentageTimepoint: Mean beck depression score is ten calculated in percentage—

Secondary

MeasureTime frame
TimePoints Events,variables,experience of secondary symptoms,signs,symptoms,age,laboratory,ultrasonographic assessment,experience of secondary intense,or different events measured at time pointsTimepoint: If five years primary outcome ,then one and three years is secondary outcome—

Countries

India

Contacts

Public ContactDr Wasia naveed

Government nizamia tibbi college and general hospital

wasia_naveed@gmail.com9394778847

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026