A study of Comparison of analgesic efficacy of superficial cervical plexus block versus clavipectoral fascia block for perioperative pain management in clavicular surgery

Comparison of analgesic efficacy of superficial cervical plexus block versus clavipectoral fascia block for perioperative pain management in clavicular surgery - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/10/075118

Enrollment

Registered

2024-10-11

Start date

Unknown

Completion date

Unknown

Last updated

2024-10-14

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

Conditions

Health Condition 1: M80-M85- Disorders of bone density and structure Health Condition 2: O- Medical and Surgical Health Condition 3: M843- Stress fracture

Interventions

Intervention1: superficial cervical plexus block or clavipectoral fascia block: In all patients posted for clavicular surgery, General anaesthesia will be given as per standard protocol. after General

Eligibility

Inclusion criteria

Inclusion criteria: 1.ASA grade I or II fit patients. 2. Ages between 18 and 65 years 3. Patients undergoing clavicle surgeries. 4. Haemodynamically stable patients with all routine investigations within normal limits without any other co morbidities. 5. Patients who are not on any cardiac related drugs. 6. Availability of written informed consent from concerned patient.

Exclusion criteria

Exclusion criteria: 1. Patients not willing to participate in this study. 2. Patients with ASA physical status III and above physical status. 3. Patients less than 18 years and above 65 years of age. 4. Patients with uncontrolled systemic disorders like neurological, cardiac, metabolic, renal, pulmonary disorders, hepatic disease with coagulation abnormalities etc. 5.Patients having local infection at the site where needle for block was to be inserted 6.Patients with bleeding or coagulation disorders. 7.Patients with known allergies to the study drugs.

Design outcomes

Primary

Measure	Time frame
Comparison of analgesic efficacy of superficial cervical plexus block versus clavipectoral fascia block for perioperative pain management in clavicular surgery by administration of Bupivacaine comparison between the two groups Post operative pain scores (VAS)and Time to first rescue analgesia will be assesssed. Timepoint: After administration of the block ,comparison between the two groups of duration of analgesia, Post operative pain scores (VAS) at 8,12,16,20,24 hrs,Time to first rescue analgesia will be assesssed.	—

Measure

Time frame

Comparison of analgesic efficacy of superficial cervical plexus block versus clavipectoral fascia block for perioperative pain management in clavicular surgery by administration of Bupivacaine comparison between the two groups Post operative pain scores (VAS)and Time to first rescue analgesia will be assesssed. Timepoint: After administration of the block ,comparison between the two groups of duration of analgesia, Post operative pain scores (VAS) at 8,12,16,20,24 hrs,Time to first rescue analgesia will be assesssed.

—

Secondary

Measure	Time frame
Comparison of analgesic efficacy of superficial cervical plexus block versus clavipectoral fascia block for perioperative pain management in clavicular surgery by perineural administration of Bupivacaine.Timepoint: After primary outcome comparison between the two groups of duration of analgesia & time to first rescue analgesia within 24 hr will also be assesssed.	—

Countries

India

Contacts

Public ContactDr. Aparna Bagle

DR.D.Y.Patil Medical College, Hospital and Research Centre, Pune

draparnabagle@gmail.com9834430811

Outcome results

None listed

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