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A randomised control trial comparing efficacy of conventional care vs enhanced recovery protocol for children undergoing surgery for developmental dysplasia of hip

Enhanced Recovery After Surgery (ERAS) pathways versus Conventional care of children undergoing surgery for Developmental Dysplasia of Hip- A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/11/047352
Enrollment
44
Registered
2022-11-16
Start date
Unknown
Completion date
Unknown
Last updated
2022-11-21

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Enhanced Recovery after Surgery (ERAS) Pathway: Pre-admission-One to One educational session with infographic poster and video, Demonstration of Spica care with spica doll, Pre-Anesthet

Sponsors

Akash Kumar Ghosh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Pediatric patients, age group between 18 months to 4 years, diagnosed with idiopathic DDH, after failed non-operative treatment, planned for Open Reduction with or without pelvic osteotomy. 2. Unilateral Single stage surgery for bilateral DDH.

Exclusion criteria

Exclusion criteria: 1. Patients with neurogenic dislocation of hip 2. Patients with age 5years 3. DDH patients with syndromic association

Design outcomes

Primary

MeasureTime frame
Post-operative pain will be assessed and recorded on the Revised Face, Legs, Activity, Crying and Consolability (FLACC) scaleTimepoint: Post-operative pain will be assessed and recorded on the Revised Face, Legs, Activity, Crying and Consolability (FLACC) scale at post-operative days 1, 2 and 4

Secondary

MeasureTime frame
Complications like wound infection, spica breakage, pressure sores, loss of reduction, pin tract infection, if present, will be recorded.Timepoint: 2 weeks, 6 weeks, 8 weeks and 3 months post-operatively.;Parental anxiety will be assessed prior to surgery with the help of the State-Trait Anxiety Inventory (STAI)scale.Timepoint: on the night prior to the surgery.;parental satisfaction will be recorded with the help of Swedish Parental Satisfaction QuestionnaireTimepoint: 3 months post-operatively.

Countries

India

Contacts

Public ContactAkash Kumar Ghosh

Postgraduate Institute of Medical Education and Research , Chandigarh

dr.nirmalraj78@gmail.com9914209740

Outcome results

None listed

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