Skip to content

A randomized control trial to assess the role of Camylofin Dihydrochloride in acceleration of active phase of labour in tertiary care hospital

A randomized control trial to assess the role of Camylofin Dihydrochloride in acceleration of active phase of labour in tertiary care hospital

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/10/046883
Enrollment
114
Registered
2022-10-28
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Health Condition 1: O30-O48- Maternal care related to the fetus and amniotic cavity and possible delivery problems

Interventions

Intervention1: Camylofin dihydrochloride: interventional drug is antispasmodic drug single dose of 1 ml drug will be injected im at 5cm of dilatation till delivery Control Intervention1: nil: nil

Sponsors

Nil
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: primigravidas in age group of 18-35 years with gestational age of 37-40 weeks with singleton foetus in vertex presentation, in active phase of labour. (Active phase of labour- 5cm or more cervical dilatation with uterine contractions.

Exclusion criteria

Exclusion criteria: any antenatal pregnancy complications like preeclampsia, eclampsia , suspected cephalopelvic disproportion, premature rupture of membranes, placenta previa, abruptio placenta, abnormal presentation, preterm labour, multiple pregnancy and patients requiring induction or use of any oxytocic drugs and any other medical disorders like diabetes, cardiac, renal and hepatic disorders. Known hypersensitivity to drugs will be excluded

Design outcomes

Primary

MeasureTime frame
to hasten the process of labour and to see the effect on cervical dilatattion rateTimepoint: from intervention to delivery

Secondary

MeasureTime frame
nausea, vomitting, dryness of mouth and tachycardiaTimepoint: from intervention to 24 hours after dlivery

Countries

India

Contacts

Public ContactThacker Shriya Himmat

Krishna institute of medical sciences karad

drhemadhumale@gmail.com9408537499

Outcome results

None listed

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