We will study the effect of superficial cervical plexus block on pain relief after surgery of thyroid gland under general anaesthesia.

Effect of bilateral superficial cervical plexus block on postoperative analgesia in thyroid surgery under general anaesthesia Randomized controlled trial - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/05/086460

Enrollment

Registered

2025-05-06

Start date

Unknown

Completion date

Unknown

Last updated

2025-05-26

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

Conditions

Health Condition 1: E071- Dyshormogenetic goiter

Interventions

Intervention1: Bilateral superficial cervical plexus block: In cases of thyroid surgery under general anaesthesia we will block bilateral superficial cervical plexus, and will observe for pain in post

Eligibility

Inclusion criteria

Inclusion criteria: ASA physical status I and II Weight more than 30Kgs Age 18 to 65 years Patients with informed and written consent

Exclusion criteria

Exclusion criteria: Any local infection at the site of giving the block Known allergy to local anaesthetic agent

Design outcomes

Primary

Measure	Time frame
To assess the time of requirement of rescue analgesia in post operative periodTimepoint: Till 24 hour after end of surgery	—

Secondary

Measure	Time frame
To evaluate the vital parameters NIBP SPO2 HR intraoperatively & postoperatively till the requirement of rescue analgesia To evaluate PONV & pain using verbal analogue scale in two groups till the requirement of rescue analgesia Timepoint: Intraop vitals at 5 10 15 20 25 30 35 40 45 50 minutes interval till the end of surgery VAS score every 2 hour for first 8 hour then after 4 hourly till 24 hour	—

Measure

Time frame

To evaluate the vital parameters NIBP SPO2 HR intraoperatively & postoperatively till the requirement of rescue analgesia To evaluate PONV & pain using verbal analogue scale in two groups till the requirement of rescue analgesia Timepoint: Intraop vitals at 5 10 15 20 25 30 35 40 45 50 minutes interval till the end of surgery VAS score every 2 hour for first 8 hour then after 4 hourly till 24 hour

—

Countries

India

Contacts

Public ContactDr Priyanka Shrivastava

Rajendra Institute of Medical Science Ranchi Jharkhand India 834009

drazizulhaque61@gmail.com8092759512

Outcome results

None listed

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