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Study of Anaesthesia Care and Outcomes in Newborns Undergoing Emergency Surgery for Birth Defects.

A Prospective Observational Study of Anaesthetict Management, Morbidity and Mortality in Neonatal Emergency Surgeries for Congenital Anomalies - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/06/111565
Enrollment
150
Registered
2026-06-01
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Health Condition 1: Q038- Other congenital hydrocephalus Health Condition 2: Q057- Lumbar spina bifida without hydrocephalus Health Condition 3: Q321- Other congenital malformations oftrachea Health Condition 4: Q390- Atresia of esophagus without fistula Health Condition 5: Q391- Atresia of esophagus with tracheo-esophageal fistula Health Condition 6: Q392- Congenital tracheo-esophageal fistula without atresia Health Condition 7: Q400- Congenital hypertrophic pyloric stenosis Health Condition 8:

Interventions

Intervention1: NIL: NIL Intervention2: Nil: Nil Intervention3: Nil: Nil

Sponsors

Maharana Bhopal Government Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All neonates from day 1 to 28 days of age, both male and female, undergoing emergency surgical procedures for congenital anomalies during the study period and whose parents provide informed consent.

Exclusion criteria

Exclusion criteria: Neonates undergoing elective surgery. Parents or legal guardians refusing consent. Neonates with incomplete data or who expire in preoperative period. Patients lost to follow up.

Design outcomes

Primary

MeasureTime frame
To evaluate the anaesthetic management and its association with perioperative morbidity and mortality in neonates undergoing emergency surgery for congenital anomalies.Timepoint: To evaluate with in 30 days postoperatively.

Secondary

MeasureTime frame
To identify perioperative factors contributing to adverse outcomes in this study population.Timepoint: Preoperative period, intraoperative period, immediate postoperative period for first 24 hours, at discharge, & postoperative day 30.;Incidence rates of congenital anomalies requiring emergency surgeries among neonates delivered at our institute & in respect to demographic area.Timepoint: At enrolment of each eligible neonate during the 12 month study period.

Countries

India

Contacts

Public ContactRitika Kumari

RNT Medical College and MB Government hospital

drlalitkumar@hotmail.com9414352823

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026