The reduction of postoperative pain in laparoscopic live donor nephrectomy after bupivacaine instillation at renal bed

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

TCTR

Registry ID

TCTR20150330001

Enrollment

Registered

2015-03-30

Start date

2015-04-01

Completion date

Unknown

Last updated

2026-08-03

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

Conditions

postoperative pain laparoscopic donor nephrectomy bupivacaine instillation postoperative pain

Interventions

NSS instillation,Bupivacaine instillation at renal bed

Placebo Comparator Drug,Experimental Drug

NSS,Bupivacaine

Eligibility

Sex/Gender

All

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: The patients who undergo laparoscopic live donor nephrectomy

Exclusion criteria

Exclusion criteria: drug allergy of acetaminophen, bupivacaine, opioids unable to evaluate pain score

Design outcomes

Primary

Measure	Time frame
The reduction of postoperative analgesia within 72 hours total amount of analgesic drugs	—

Secondary

Measure	Time frame
The reduction of postoperative pain within 72 hours pain score	—

Countries

Thailand

Contacts

Public ContactChalairat Suk-ouichai

Siriraj Hospital

chalainok@yahoo.com66869782178

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026