Use of anaesthesia Drugs in PECS block for modified radical mastectomy.

To Evaluate the efficacy of PECS block as standalone anaesthesia technique for modified radical mastectomy- A Prospective interventional study. - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/11/097985

Enrollment

Registered

2025-11-24

Start date

Unknown

Completion date

Unknown

Last updated

2025-12-08

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

Conditions

Health Condition 1: C509- Malignant neoplasm of breast of unspecified site

Interventions

Intervention1: PECS I AND PECS II Block using 0.5% Ropivacaine with dexamethasone with dexmedetomidine infusion for sedation.: Ultrasound-guided PECS I and II blocks will be performed using 30 mL of 0

Eligibility

Inclusion criteria

Inclusion criteria: Patients classified as American Society of Anaesthesiologists (ASA) physical status I, II OR III.

Exclusion criteria

Exclusion criteria: 1. Patient refusal to participate or undergo regional anesthesia. 2.Known allergy or hypersensitivity to local anesthetics or study drugs (Ropivacaine, dexamethasone, fentanyl, dexmedetomidine,bupivacaine). 3.Infection at the block site or local skin pathology. 4. Coagulopathy or bleeding disorders 5.History of severe cardiovascular or respiratory instability contraindicating sedation or regional anesthesia. 6. Neurological disorders affecting pain perception or sensory mapping. 7. Patients on chronic opioid or sedative use, which may influence block efficacy. 8.Inability to understand or communicate pain scores reliably (e.g., severe cognitive impairment). 9.BMI more than 35 kg per m , as excessive adiposity may interfere with block performance or ultrasound visualization

Design outcomes

Primary

Measure	Time frame
TO assess the success rate of surgeries completed without conversion to general anaesthesia. 2.Assessing the requirement of intraoperative opiod - fentanyl.Timepoint: Before block, just after block ,then every 5 min. till 30 mins and then 1 hrly till the end of surgery	—

Secondary

Measure	Time frame
1. To assess the intraoperative hemodynamic stability and document any complications or adverse events related to PECS block or sedation. 2.To determine the duration of postoperative analgesia.Timepoint: To observe postoperative pain scores using NRS at 1,2,4,8,12 and 24 hours	—

Countries

India

Contacts

Public ContactDr Kanta Bhati

Sardar Patel Medical College Bikaner, Rajasthan, India

drkantabhati67@gmail.com9413466688

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026