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NCT03965442
Effects of Intraoperative Esmolol on Post-mastectomy Pain Syndrome
trial testing Control in Post-mastectomy Pain Syndrome in 66 participants. Status unknown.
31 July 2019
Quick facts
| Lead sponsor | Hospital de Base |
|---|---|
| Status | Status unknown |
| Study type | OBSERVATIONAL |
| Enrollment | 66 |
| Start date | 1 January 2019 |
| Primary completion | 31 July 2019 |
| Estimated completion | 31 July 2019 |
| Sites | 1 location across Brazil |
Drugs / interventions tested
- Control
- Esmolol (ESMOLOL) — full drug profile →
Conditions studied
- Post-mastectomy Pain Syndrome — all drugs for Post-mastectomy Pain Syndrome →
Sponsor
Hospital de Base
Who can join
Adults 18 to 65, female only, with Post-mastectomy Pain Syndrome. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Chronic postoperative pain is an entity that is usually neglected by anesthetists, but several studies show that the choice of anesthetic technique may interfere with this prevalence. Esmolol is a selective beta-blocker of ultra fast duration that has been studied as a perioperative venous adjuvant with antihyperalgesic and opioid sparing action. The investigators ventured the possibility of this anti-hyperalgesic effect attenuating the chronic pain syndrome post-mastectomy.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT03965442
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other recruiting trials for Post-mastectomy Pain Syndrome
Currently open trials in the same condition.
- NCT04874038 — Prevention of Persistent Pain With LidocAine iNfusions in Breast Cancer Surgery (PLAN) · Phase 3 · recruiting
Other Hospital de Base trials
Trials by the same sponsor.
- NCT07032012 — Impact of Pre-anesthetic Evaluation on the Anxiety · NA · not yet recruiting
- NCT06836622 — Carotid-Femoral, Oscillometric and Estimated Pulse Wave Velocity · enrolling by invitation
- NCT03932422 — Central Hemodynamic and Sodium Urinary · unknown
- NCT03612492 — The Effects of Lidocaine and Esmolol on Attenuation of Hemodynamic Response to Orotracheal Intubation · Phase 4 · unknown
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 NCT03965442 (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 Hospital de Base
- Last refreshed: 29 May 2019
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/NCT03965442.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing