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Effects and safety of ketorolac tromethamine or dexamethasone combined with ropivacaine in transverse abdominis plane block after gynecological single hole laparoscopic surgery

Effects and safety of ketorolac tromethamine or dexamethasone combined with ropivacaine in transverse abdominis plane block after gynecological single hole laparoscopic surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500098950
Enrollment
Unknown
Registered
2025-03-17
Start date
2025-03-20
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

Gynecological patients with single hole laparoscopy

Interventions

Ketorolac tromethamine group:Ketorolac tromethamine 60mg+0.25% ropivacaine hydrochloride injection mixture 40ml.
Dexamethasone group:Dexamethasone 10mg+0.25% ropivacaine hydrochloride injection mixture 40ml.
Control group:0.25% ropivacaine hydrochloride 40ml

Sponsors

Zigong Maternal and Child Health Care Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Gynecological single hole laparoscopic surgery; 2. Aged 18-65 years; 3. American Society of Anesthesiologists (ASA) classification I-III.

Exclusion criteria

Exclusion criteria: 1. Patients with a history of allergy to local anesthetics; 2. Patients with a history of allergy to ketorolac tromethamine and aspirin or other non-steroidal anti-inflammatory drugs; 3. Patients with active peptic ulcer, recent gastrointestinal bleeding or perforation, and with a history of peptic ulcer or gastrointestinal bleeding; 4. Patients with renal failure caused by renal function injury and insufficient blood volume; 5. Patients with suspected or diagnosed cerebrovascular hemorrhage, bleeding tendency, incomplete hemostasis and high-risk hemorrhage; 6. Patients with a history of allergy to dexamethasone.

Design outcomes

Primary

MeasureTime frame
Incidence of moderate to severe pain in 24 hours ;

Secondary

MeasureTime frame
BCS comfort score within 48 hours after surgery;Consumption of analgesic drugs and analgesia rescue rate;QoR-15 scale evaluation ;Incidence of postoperative nausea and vomiting;Perioperative blood glucose changes;

Countries

China

Contacts

Public ContactLina Wang

Zigong Maternal and Child Health Care Hospital

413071034@qq.com+86 158 0822 9636

Outcome results

None listed

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