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Comparison of hydromorphone and sufentanil for pain control in paediatrics after surgery: a random double blind, controlled, prospective study

Comparison of hydromorphone and sufentanil for pain control in paediatrics after surgery: a random double blind, controlled, prospective study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-15007641
Enrollment
Unknown
Registered
2015-12-23
Start date
2016-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Developmental dysplasia of the hip

Interventions

Control Group:Sufentanil Citrate injection PCIA
Experimental Group:Hydromorphone hydrochloride injection PCIA

Sponsors

Department of Aensthesiology and Surgery, The Second Hospital l of Lanzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 5 Years

Inclusion criteria

Inclusion criteria: 1. ASA I or II; 2. aged 2-5 years; 3. Developmental dysplasia of the hip repair surgery under general anesthesia; 4. Participate in the trial after families consent; 5. Accord with conditions of general anesthesia.

Exclusion criteria

Exclusion criteria: 1. Serious congenital heart disease untreated; 2. Difficult airway; 3. Contraindications or allergy to opioid drugs; 4. Poor collaboration of paents; 5. Researchers think that there are inappropriate factors for selected conditions.

Design outcomes

Primary

MeasureTime frame
Resting and Moving FLACC scores;The time of FLACC reduced to less than 4;Additional numbers of blous;

Secondary

MeasureTime frame
Satisfaction of the anagesia;The observers assessment of sedation scale;Post-operative hospital stay;Behavior changes of postoperation;

Countries

China

Contacts

Public ContactSHI Yisa
shiys@lzu.edu.cn+86 13619334024

Outcome results

None listed

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