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Intrathecal Hydromorphone versus Intrathecal Morphine for Analgesia after laparoscopic hepatectomy

Intrathecal Hydromorphone versus Intrathecal Morphine for Analgesia after laparoscopic hepatectomy

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300070888
Enrollment
Unknown
Registered
2023-04-25
Start date
2023-05-02
Completion date
Unknown
Last updated
2023-06-04

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

Conditions

liver tumor

Interventions

the group of hydromorphone:After successful subarachnoid puncture, 75 ug hydromorphone is administrated.
the group of morphine:After successful subarachnoid puncture, 150ug morphine is administrated.

Sponsors

Sir Run Run Shaw Hospital (SRRSH), affiliated with the Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. American Society of Anesthesiologists physical status I and II; 2. patients scheduled for laparoscopic liver resection surgery; 3. age between 18-75; 4. body mass index <=30 kg/m2; 5. Volunteered to participate in this study, and signed informed consent was obtained

Exclusion criteria

Exclusion criteria: 1. Hypersensitivity to hydromorphone and morphine or its excipient ingredients; 2. Had contraindications to spinal anesthesia; 3. Had taken or were recently taking opioids, non steroidal anti-inflammatory drugs 48 h before surgery 4. Had severe cardiocerebral hepatic and renal dysfunction, bronchial asthma, endocrine disease, dysuria, ileus as well as severe infectious disease; 5. Suspected or true history of alcohol, drug abuse; 6. History of substance abuse, chronic pain and psychiatric disorders, other concurrent diseases in pregnancy; 7. Refusal of analgesic pump; 8. Had participated in other clinical studies within 3 month; 9. Vulnerable populations, including those with psychiatric disorders, cognitively impaired, critically ill, pregnant, illiterate, etc

Design outcomes

Primary

MeasureTime frame
VAS score;

Secondary

MeasureTime frame
Time to first compression of analgesic pump;

Countries

China

Contacts

Public ContactChunyan Yan

Sir Run Run Shaw Hospital (SRRSH), affiliated with the Zhejiang University School of Medicine

yanchun-yan@163.com+86 13588706724

Outcome results

None listed

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