FindTrial
Sign In

A propensity-score matching study comparing intrathecal hydromorphone with transversus abdominis plane block for upper-abdominal surgery analgesia

A propensity-score matching study comparing intrathecal hydromorphone with transversus abdominis plane block for upper-abdominal surgery analgesia

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400079577
Enrollment
Unknown
Registered
2024-01-06
Start date
2024-01-08
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

postoperative pain

Interventions

TAP group:None
ITH group:None

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 79 Years

Inclusion criteria

Inclusion criteria: ?elective upper abdominal surgery; ?Intrathecal injection analgesia, or one or more peripheral block analgesia (including transversus abdominis plane block, rectus sheath block, serratus anterior block); ?ASA grade II-III.

Exclusion criteria

Exclusion criteria: The operation time is less than 2 hours.

Design outcomes

Primary

MeasureTime frame
the moderate to severe pain at rest or during movement;—

Secondary

MeasureTime frame
the moderate to severe pain at rest or during movement;the numerical rating scores at rest or during movement;the numerical rating scores at rest or during movement;postoperative nausea and vomiting, PONV;postoperative pruritus;respiratory depression;first day opioids consumption;postoperative length of stay;satisfaction score;—

Countries

China

Contacts

Public ContactFei Liu

West China Hospital, Sichuan University

30333870@qq.com+86 189 8060 5856

Outcome results

None listed

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