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TPVB, PECSB, ESPB for Postmastectmy Pain (RCT)

M

Menoufia University

Status

Completed

Conditions

Pain, Postoperative

Treatments

Drug: IV morphine
Procedure: Ultrasound guided block

Study type

Interventional

Funder types

Other

Identifiers

NCT05076773
32900654326

Details and patient eligibility

About

Aim of the work The aim of the study is to compare between the effects of ultrasound guided thoracic paravertebral block, pectoral nerve block II, and erector spinae block in management of pain during cancer breast surgeries. The hypothesis of the study is that the three groups will give comparative results.

Enrollment

80 patients

Sex

Female

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. ASA physical status classification class I or II
  2. Age group 18 - 60 years of the female gender
  3. Patients undergoing breast cancer surgeries

Exclusion criteria

  1. Patient refusal
  2. History of hypersensitivity to local anesthetics
  3. Bleeding disorders or patients receiving anticoagulants
  4. Spine or chest wall deformities
  5. Pregnancy
  6. Local infection at the site of injection.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

80 participants in 4 patient groups, including a placebo group

Control Group (D)
Placebo Comparator group
Description:
Patient will receive opioid only for management of their perioperative pain
Treatment:
Drug: IV morphine
Paravertebral block Group (A)
Active Comparator group
Description:
Will receive thoracic paravertebral block
Treatment:
Procedure: Ultrasound guided block
Drug: IV morphine
Pectoral block Group (B)
Active Comparator group
Description:
Will receive pectoral 1 and 2 block
Treatment:
Procedure: Ultrasound guided block
Drug: IV morphine
Erector spinae block Group (C)
Active Comparator group
Description:
Will receive erector spinae block
Treatment:
Procedure: Ultrasound guided block
Drug: IV morphine

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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