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The Application of Pectoral Nerve II(PECS II)block in Breast Fibroadenoma Resection Surgery

I

Inner Mongolia Baogang Hospital

Status

Completed

Conditions

Breast Neoplasms

Treatments

Drug: nerve block with 0.5% ropivacaine

Study type

Interventional

Funder types

Other

Identifiers

NCT06608810
2024-MER-069

Details and patient eligibility

About

Patients were randomly assigned to the GA group, PECS II group, or TPVB group using a computer-generated random number table. Group assignments were kept in a sealed envelope, which was opened only after induction of general anesthesia on the day of surgery. This study was a double-blind trial, ensuring that neither the patients nor the investigators were aware of the analgesic method used. The same anesthesiologist was responsible for PECS II block or TPVB, while different anesthesiologists were responsible for anesthesia implementation and postoperative follow-up.

Full description

Written informed consent was obtained from all participants.90 female patients aged 18 to 65 with ASA I-II status were selected at Baogang Hospital, Inner Mongolia, who had been diagnosed with breast fibroadenomas. Exclusion criteria included pre-existing infection at the site of block, coagulation disorders, morbid obesity (body mass index > 40 kg/m²), allergy to local anesthetics, impaired lung function, significant cardiac disease, renal dysfunction, pre-existing neurological disorders, and psychiatric conditions.

Enrollment

90 patients

Sex

Female

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Clinical diagnosis of breast fibromas

Exclusion criteria

  • heart attack mental disorder

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

90 participants in 1 patient group

Comparison of efficacy in pectoral nerve block type II, thoracic paravertebral block, and general an
Other group
Treatment:
Drug: nerve block with 0.5% ropivacaine

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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