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NCT03335410
The Recuperation of Patients After Elective Shoulder Surgery Observational Cohort Study
trial testing Non- interventional in Aucte Pain After Surgery in 122 participants. Completed in 15 January 2018.
15 January 2018
Quick facts
| Lead sponsor | Tampere University Hospital |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 122 |
| Start date | 15 September 2017 |
| Primary completion | 15 January 2018 |
| Estimated completion | 15 January 2018 |
| Sites | 14 locations across Finland |
Drugs / interventions tested
- Non- interventional
Conditions studied
- Aucte Pain After Surgery — all drugs for Aucte Pain After Surgery →
- Persistent Pain After Surgery — all drugs for Persistent Pain After Surgery →
- Opioid Use After Surgery — all drugs for Opioid Use After Surgery →
- Mode of Anaesthesia — all drugs for Mode of Anaesthesia →
Sponsor
Tampere University Hospital
Who can join
Adults 18 to 85, any sex, with Aucte Pain After Surgery or Persistent Pain After Surgery. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Around 6400 shoulder surgeries are performed yearly in Finland. The procedure is mainly day-case surgery and the patients go home in the afternoon. Shoulder surgery is one of the most common procedures performed in private surgical practices. Because of the complex nature of the joint, the recovery may be complicated by severe opstoperative pain, which is relieved with strong opioids. Recently this has been addressed in the literature, as prescribed opioids too often lead to substance abuse. Pain in the acute phase after surgery is one of the common risk factors for persistent postoperative pain, which is a major burden for both the individual patient and the society. In this prospective, observational cohort study we aim to describe current standards of practice in planning and taking care of anaeshtesia and prescribing opioids and adjuvants for postoperative pain relief at home.
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 NCT03335410
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
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Trials by the same sponsor.
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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 NCT03335410 (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 Tampere University Hospital
- Last refreshed: 6 September 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/NCT03335410.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing