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NCT07429916

Ketamine for Shoulder Pain Following Laparoscopic Gastric Sleeve Surgery

Recruiting now EARLY_PHASE1 Last updated 24 February 2026
What this trial tests

EARLY_PHASE1 trial testing Intraoperative ketamine in Pain Management in 50 participants. Currently enrolling.

Timeline
1 January 2026
Primary endpoint
30 June 2026
30 August 2026

Quick facts

Lead sponsorKing Abdullah University Hospital
PhaseEARLY_PHASE1
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment50
Start date1 January 2026
Primary completion30 June 2026
Estimated completion30 August 2026
Sites1 location across Jordan

Drugs / interventions tested

Conditions studied

Sponsor

King Abdullah University Hospital

Who can join

Adults 18 to 60, any sex, with Pain Management or Laparascopic Sleeve Gastrectomy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Shoulder pain is a well-recognized complaint following laparoscopic surgery. It is underlying mechanism has various causes, therefore, modalities in management and prevention of this sort of pain are numerous with different success rates. In the light of this, the investigators aim to compare an anesthetic management plan involving using ketamine (which is a known intraoperative anesthetic agent) to another not involving it for participants undergoing gastric sleeve, and compare the incidence and intensity of shoulder pain afterwards.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Pain Management

Currently open trials in the same condition.

Other King Abdullah University Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07429916.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing