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NCT04162951
Retrolaminar Thoracic Paravertebral Block
NA trial testing Ordinary approach paravertebral block in Regional Anesthesia Morbidity in 93 participants. Completed in 19 October 2023.
19 October 2023
Quick facts
| Lead sponsor | Tanta University |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | triple |
| Primary purpose | supportive care |
| Enrollment | 93 |
| Start date | 10 November 2019 |
| Primary completion | 19 October 2023 |
| Estimated completion | 19 October 2023 |
| Sites | 1 location across Egypt |
Drugs / interventions tested
- Ordinary approach paravertebral block
- Retrolaminar paravertebral block
Conditions studied
- Regional Anesthesia Morbidity — all drugs for Regional Anesthesia Morbidity →
- Postoperative Pain — all drugs for Postoperative Pain →
Sponsor
Tanta University
Who can join
Adults 40 to 60, female only, with Regional Anesthesia Morbidity or Postoperative Pain. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This clinical study will be conducted on female patients admitted to The General Surgery Department of Tanta Faculty of Medicine for a period of 9 months. Patients will be randomly allocated into one of the following two groups;- • Ordinary approach group (30 patients): The patients in this group will receive ordinary ultrasound-guided thoracic paravertebral block. • Retro-laminar approach group (30 patients): The patients in this group will be receive real ultrasound-guided Retrolaminar thoracic paravertebral block. All the patients will receive general anesthesia with attachment to a monitor (5 ASA Monitoring) In addition to bispectral index.
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 NCT04162951
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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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 NCT04162951 (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 Tanta University
- Last refreshed: 24 October 2023
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/NCT04162951.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing