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NCT04676438
Persistant Post-mastectomy Pain in Breast Cancer : Incidence and Risk Factors
trial in Breast Neoplasms in 722 participants. Completed in 7 March 2021.
8 September 2020
Quick facts
| Lead sponsor | Moroccan Society of Surgery |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 722 |
| Start date | 10 December 2018 |
| Primary completion | 8 September 2020 |
| Estimated completion | 7 March 2021 |
| Sites | 2 locations across Morocco |
Conditions studied
- Breast Neoplasms — all drugs for Breast Neoplasms →
- Pain, Postoperative — all drugs for Pain, Postoperative →
- Pain, Chronic — all drugs for Pain, Chronic →
Sponsor
Moroccan Society of Surgery
Who can join
18 and older, female only, with Breast Neoplasms or Pain, Postoperative. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Post Mastectomy Pain Syndrome (PMPS) is a major complication of breast surgery responsible for depression and disability. The project consists of a prospective cohort on patients going for oncological breast surgery at National Institute of Oncology of Rabat. Chronic postoperative pain (CPP) remains a disturbing and obscure clinical problem, which could last for more than 3 months after surgery. The aim of present study was to assess the prevalence of CPP, investigate its impact on life quality and explore its potential risk factors. After informed consent was signed, patients receiving surgery under general anesthesia in Peking Union Medical College Hospital and other medical centers participating in this study during 2018 will be included. Patients' preoperative information will be collected from medical record, including basic demographic data, primary disease and previous chronic diseases. Intraoperative information will be obtained from anesthesia record, including surgical scope, duration, length and location of incisions and blood loss. Acute pain will be evaluated in the ward of the department of surgery, when an app will be installed on patients' mobile phones. Our long-term postoperative follow-up would be performed by sending out survey questionnaires via this app in the 4th, 8th, 16th, 32th, and 48th weeks after surgery. The survey covers questions regarding the intensity, characteristic, location and impact on daily activities of CPP. Information regarding treatment of CPP will also be collected, if any. All the data gained will be summarized in our database and analyzed.
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 NCT04676438
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Moroccan Society of Surgery trials
Trials by the same sponsor.
- NCT04607577 — Cross-cultural Adaptation and Validation in Moroccan Arabic Dialect "Darija" of the QoR-15 Postoperative Recovery Qualit · unknown
- NCT05494281 — Serratus Anterior Plane Block to Prevent Chronic Postoperative Pain in Breast Cancer · NA · unknown
- NCT04130568 — Translation and Adaptation of Learning Organisation Survey for French Speaking Countries · completed
- NCT04000802 — Evaluation of the Decision-making During Multidisciplinary Meetings for Digestive Cancers · completed
- NCT05286411 — Evaluation of the Implementation of a Quality Improvement Program Through Morbidity and Mortality Reviews · completed
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 NCT04676438 (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 Moroccan Society of Surgery
- Last refreshed: 20 July 2021
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/NCT04676438.
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