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NCT03585088
The Prediction for Postoperative Pain
NA trial testing surgical pleth index in Pain, Postoperative in 53 participants. Completed in 19 October 2018.
19 October 2018
Quick facts
| Lead sponsor | Samsung Medical Center |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 53 |
| Start date | 30 June 2018 |
| Primary completion | 19 October 2018 |
| Estimated completion | 19 October 2018 |
| Sites | 1 location across South Korea |
Drugs / interventions tested
- surgical pleth index
Conditions studied
- Pain, Postoperative — all drugs for Pain, Postoperative →
- Nociceptive Pain — all drugs for Nociceptive Pain →
- Analgesia, Patient-Controlled — all drugs for Analgesia, Patient-Controlled →
- Analgesics — all drugs for Analgesics →
Sponsor
Samsung Medical Center
Who can join
Adults 20 to 80, any sex, with Pain, Postoperative or Nociceptive Pain. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
If the individual patient's pain is assessed and the amount of analgesic needed after surgery is predicted, appropriate injection of pain control and excessive injection of narcotic analgesic can be prevented. Therefore, investigators try to evaluate the degree of pain during surgery and the amount of analgesic use for management of postoperative pain.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT03585088
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of surgical pleth index
Trials testing the same drug.
- NCT03417180 — SPI-guided Analgesia During FESS for Intraoperative Blood Loss · NA · unknown
Other recruiting trials for Pain, Postoperative
Currently open trials in the same condition.
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Other Samsung Medical Center trials
Trials by the same sponsor.
- NCT07482865 — Routine Versus Provisional Distal Perfusion Catheter Placement in Patients Undergoing Mechanical Circulatory Support · NA · not yet recruiting
- NCT07467213 — Routine Use of Potassium Competitive Acid Blocker vs. Guideline-Directed Gastrointestinal Protection Strategy in Acute M · Phase 4 · not yet recruiting
- NCT07530913 — Effectiveness Analysis of a Rehabilitation Exercise Platform for Living Donor Liver Transplantation Patients · NA · enrolling by invitation
- NCT07500701 — Salvage Moderate Hypofractionated Versus Ultrahypofractionated Radiotherapy for Biochemical Recurrence After Radical Pro · Phase 3 · recruiting
- NCT07409441 — Korea Acute Myocardial Infarction Registry · not yet recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03585088 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Samsung Medical Center
- Last refreshed: 26 October 2018
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/NCT03585088.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing