NCT03614091 is a NA clinical trial of Erector spinae plane block in Pain, Postoperative, sponsored by Assiut University.

Who is sponsoring NCT03614091?

NCT03614091 is sponsored by Assiut University.

What drugs are being tested in NCT03614091?

Interventions in NCT03614091: Erector spinae plane block, Paravertebral plane block.

What condition does NCT03614091 study?

NCT03614091 studies Pain, Postoperative, Pulmonary Atelectasis, Mastectomy.

Is NCT03614091 still recruiting?

NCT03614091 is currently completed. Last updated 26 June 2024.

Last reviewed 2024-06-26 · How we verify

NCT03614091

Name: Drug Landscape Pharmaceutical Database
Creator: Drug Landscape
Published: 2026-01-01
License: https://creativecommons.org/licenses/by/4.0/

Paravertebral Block Versus Erector Spinae Plane Block for Modified Radical Mastectomy in Womens.

Completed NA Last updated 26 June 2024

What this trial tests

NA trial testing Erector spinae plane block in Pain, Postoperative in 40 participants. Completed in 27 December 2023.

Timeline

1 February 2020

Primary endpoint
5 April 2023

27 December 2023

Quick facts

Lead sponsor	Assiut University
Phase	NA
Status	Completed
Study type	INTERVENTIONAL
Allocation	randomized
Design	parallel
Masking	double
Primary purpose	prevention
Enrollment	40
Start date	1 February 2020
Primary completion	5 April 2023
Estimated completion	27 December 2023
Sites	1 location across Egypt

Drugs / interventions tested

Erector spinae plane block — full drug profile →
Paravertebral plane block

Conditions studied

Pain, Postoperative — all drugs for Pain, Postoperative →
Pulmonary Atelectasis — all drugs for Pulmonary Atelectasis →
Mastectomy — all drugs for Mastectomy →

Sponsor

Assiut University

Who can join

Adults 18 to 50, female only, with Pain, Postoperative or Pulmonary Atelectasis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

postoperative pain following Modified radical mastectomy is severe specially after dissection of tissues .paravertebral plane block provides an excellent postoperative analgesia for women's,but it carry the risk of pneumothorax which it reported in some cases.Erector spinae plane block is a recent block has been mentioned in many case reports as a safe,quick and can be used in outpatient setting. we use a comparative study to compare the postoperative analgesia between both blocks and the affection of postoperative pain following both blocks if any on pulmonary functions.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

A comparative study of respiratory effects of erector spinae plane block versus paravertebral plane block for women undergoing modified radical mastectomy.
Sayed JA, Hamed R, Abdelraouf AM, El-Hagagy NYM, et al · · 2024 · cited 3× · PMID 39080545 · DOI 10.1186/s12871-024-02632-4

Verify or expand the search:

Other trials of Erector spinae plane block

Trials testing the same drug.

NCT07537036 — Analgesic Efficacy of Quadro-Iliac Plane Block Versus Erector Spinae Plane in Total Hip Arthroplasty · NA · not yet recruiting
NCT07367568 — Costotransverse Foramen Block With Erector Spinae Plane Block in Modified Radical Mastectomy · NA · recruiting
NCT07278050 — Interscalene Block vs Serratus Posterior Superior Intercostal Plane Block · NA · recruiting
NCT07272577 — Erector Spinae Plane Block on Postoperative Analgesia in Patients Undergoing Laparoscopic Abdominal Surgeries · NA · recruiting
NCT07251400 — Analgesic Efficacy of Erector Spinae and Rectus Sheath Block in Patients Undergoing Laparoscopic Inguinal Hernia Repair · NA · active not recruiting

Other recruiting trials for Pain, Postoperative

Currently open trials in the same condition.

NCT07512141 — Single Versus Double Drains in the Axillary and Pectoral Regions After Modified Radical Mastectomy · NA · recruiting
NCT07354581 — Erector Spinae Plane Block vs Quadro-Iliac Plane Block After Lumbar Instrumentation Surgery · NA · recruiting
NCT07239817 — PENG Block + LIA For Endoprosthesis Surgery With Anterior Approach · NA · recruiting
NCT06740214 — Analgesic Efficacy of Different Liposomal Bupivacaine Doses in the Adductor Canal Block for Total Knee Arthroplasty · Phase 3 · recruiting
NCT07057557 — Aloe Vera vs Paraffin Tulle Dressings for Pain Management in Split Thickness Skin Graft Donor Sites · NA · recruiting

Other Assiut University trials

Trials by the same sponsor.

NCT07423312 — Lead Exposure and Multiple Sclerosis · not yet recruiting
NCT07234526 — Usage of Glucose Fluctuations as a Prognostic Marker in Septic Shock Patients · not yet recruiting
NCT07273214 — Knowledge, Attitude and Practice of Third Trimester Pregnant Mothers Towards Self-Medication in Assiut, Egypt · not yet recruiting
NCT07194863 — Efficacy of Essential Phospholipid Versus Betaine HCL/L-Glutamic Acid in MAFLD · not yet recruiting
NCT07053709 — Screening for Hyperuricemia in Patients With Metabolic Associated Fatty Liver Disease (MAFLD) · 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)

Data sources for this page

Trial protocol + status: ClinicalTrials.gov NCT03614091 (US National Library of Medicine, public domain)
Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
Sponsor: as reported to ClinicalTrials.gov by Assiut University
Last refreshed: 26 June 2024

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/NCT03614091.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing