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Erector Spinae Block in First Rib Resection: a Monocentric Before-after Study

Bloc Des Muscles Erecteurs du Rachis Pour Chirurgie d'exérèse de première côte Dans le Cadre du Syndrome du défilé Cervico-thoracique: évaluation Avant-après au CHU d'Angers.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04167046
Acronym
MERCOTE
Enrollment
60
Registered
2019-11-18
Start date
2019-11-30
Completion date
2021-03-31
Last updated
2019-11-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Thoracic Surgery

Brief summary

First rib resection surgery for thoracic outlet syndrome is associated with an intense postoperative pain. It leads to significant consumption of nonsteroidal anti-inflammatory drugs and opioids, and hospitalization for several days. In our center, first rib resection surgery was usually performed under general anesthesia combined with diffuse local infiltration of the axillary fossa. Erector spinae block is an interfascial block where a local anesthetic is injected between the erector spinae muscle and the transverse process, in order to obtain a multimetameric analgesia. It has now shown its efficacy and its safety in thoracic and abdominal surgeries by decreasing the morphine consumption and pain scores. Since November 2018, this erector spinae block is systematically performed preoperatively for first rib resection in our center, in association with a general anesthesia. Patient satisfaction seems important but remains to be assessed objectively. In a before-after study, our goal is to assess the impact of the use of erector spinae block on postoperative pain in the first rib resection surgery.

Interventions

PROCEDUREErector spinae block

Preoperative erector spinae block.

Sponsors

University Hospital, Angers
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* First rib resection for thoracic outlet syndrome

Design outcomes

Primary

MeasureTime frameDescription
Pain assessment at H+48Day 2 after surgeryNumerical pain rating scale: 0 (no pain at all) to 10 (worst imaginable pain)

Secondary

MeasureTime frameDescription
Total consumption of morphine (per and postoperative)Hour 2, Day 1, Day 2 and Day 3 after surgery
Postoperative pain assessment at other timesHour 2, Day 1, and Day 3 after surgeryNumerical pain rating scale: 0 (no pain at all) to 10 (worst imaginable pain)
Frequency of adverse effects related to morphine Frequency of morphine side effectsHour 2, Day 1, Day 2 and Day 3 after surgery
Length of hospital stayThrough study completion, an average of 1 year

Countries

France

Contacts

Primary ContactEmmanuel Rineau, MD
erineau@live.fr+33241353951
Backup ContactSiaudeau Hélène, MD
+33241353951

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026