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Assessment Effect of Bopronorphin Neonates With Obstinence Syndrom

Comparison Bopronorphin and Morphin Among NeonatesWith Obstinence Syndrom Admitted In Birjand Vali-asr Hospital

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20181231042183N1
Enrollment
60
Registered
2019-01-18
Start date
2018-12-22
Completion date
Unknown
Last updated
2019-01-29

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

Conditions

Neonatal Abstinence Syndrome. Neonatal withdrawal symptoms from maternal use of drugs of addiction

Interventions

Intervention 1: Intervention group: Randomized clinical trial study in 60 neonate. 2 group of neonatal abstinence syndrome that randomized divided to 2 group of Buprenorphine (intervention group 30 ne

Sponsors

Birjand University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Days to 7 Days

Inclusion criteria

Inclusion criteria: Postnatal Age<7 Days Gestational Age= 35 Weeks Prenatal Opium Exposure Symptomatic Patient And 3 Fingan Score =8 In 3 Hours Or 2 Fingan Score=12 No Siezure History No Major Congenital Anomaly No Unstablity In Blood Pressure And Hemodynamic No Major Medical Unstability In Association Of Withdrawal Syndrome

Exclusion criteria

Exclusion criteria: Analgesic Consumption and withdrawal syndrome

Design outcomes

Primary

MeasureTime frame
Admit Duration. Timepoint: Duration of Admit. Method of measurement: Observation of physician.;Drugs Complications. Timepoint: Admit Duration. Method of measurement: Observation of physician.;Apnea. Timepoint: Admit Duration. Method of measurement: Observation of physician.;Feeding. Timepoint: Admit Duration. Method of measurement: Observation of physician.;Blood Pressure. Timepoint: Admit Duration. Method of measurement: Mercurial Pressure-Gauge Device.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactGholamreza Faal

Birjand University of Medical Sciences

s.hajmohamadi@bums.ac.ir+98 56 3239 5000

Outcome results

None listed

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