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To assess the effect of erector spinae plane block using ultrasound in head and neck cancer surgery patients

To evaluate the analgesic effect of unilateral ultrasound guided bi-level erector spinae plane block with multimodal analgesia in patients undergoing elective head and neck cancer reconstruction surgery- a randomized control trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/12/098326
Enrollment
58
Registered
2025-12-02
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: C060- Malignant neoplasm of cheek mucosa

Interventions

Intervention1: Nil: Nil

Sponsors

Kalyan Singh Super Speciality Cancer Institute Lucknow India
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: those patients who are diagnosed with head neck cancer with PMMC flap, gave consent and of ASA I & II status will be enrolled in the study.

Exclusion criteria

Exclusion criteria: patient posted for only neck dissection or bilateral neck dissection, free flap, recurrence of tumour, allergy to LA, bleeding disorders, cervical and thoracic spine deformity, infection at block site.

Design outcomes

Primary

MeasureTime frame
to assess the intraopoerative fentanyl comsumption and to record the time in hours when first rescue analgesia will be recieved.Timepoint: 1h, 4h, 8h, 12h, 24h—

Secondary

MeasureTime frame
to assess the postoperative pain score using VAS scale and to record the block related complications and side effects.Timepoint: 1h, 4h, 8h, 12h 24h—

Countries

India

Contacts

Public ContactArchana Gautam

Kalyan Singh Super Speciality Cancer Institute Lucknow

archana.dolly76@gmail.com9936343627

Outcome results

None listed

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