Assessment of effects of superficial cervical plexus block for surgeries in head and neck region: a comparative study

Evaluation of efficacy of superficial cervical plexus block for surgeries in head and neck region:a comparative randomized control study

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2021/06/034429

Enrollment

Registered

2021-06-28

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: superficial cervical plexus block: this block provide analgesia in intraoperative and postoperative period and decrease requirement of systemic analgesic infirst 24 hours Control Interv

Eligibility

Inclusion criteria

Inclusion criteria: weight:40-75 ASA -I/II/III malampatti grade:I/II/III duration of surgery patient able to give written & informed consent patient able to understand VAS regarding assessment of pain

Exclusion criteria

Exclusion criteria: patients with coagulopathy,local infection, pre-existing neuropathy or any other neurological disease hypersensitivity to local anesthetic patient with history of drug or alcohol abuse, psychiatric illness

Design outcomes

Primary

Measure	Time frame
duration of pain relief total requirement of systemic analgesicTimepoint: every hourly after completion of ot for first 24 hours	—

Secondary

Measure	Time frame
requireement of systemic analgesic in intraoperative periodTimepoint: every 10 minutes for 1st hour, every 20 minutes for 2nd and 3rd hour	—

Countries

India

Contacts

Public Contactdr neha shah

ssg hospital

nehakinit@gmail.com9898019910

Outcome results

None listed

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