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Regional Anesthesia for Thyroidectomy

G

Guangzhou First People's Hospital

Status

Unknown

Conditions

Chronic Pain
Acute Pain

Treatments

Procedure: placebo
Procedure: nerve block

Study type

Interventional

Funder types

Other

Identifiers

NCT02108834
GZFPH-IRB-2013-085

Details and patient eligibility

About

For more than 25 years, Regional Anesthesia has challenged anesthesiologists to determine whether it offers real benefits in terms of patient outcome from major surgery, compared with general anesthesia. Although it is clear that regional analgesia in association with general anesthesia substantially reduces postoperative pain, the benefits in terms of overall perioperative outcome are controversial. The aim of this study is to evaluate the effect on short and long-term postoperative outcomes of adding regional analgesia to general anaesthesia in thoridetomic patients.

Full description

Patients who are divided into two treatment groups: (a) a bilateral superficial cervical plexus group (group S) and a control group (group C).We performe bilateral superficial cervical plexus block (BSCPB)with 0.25-0.75% ropivacaine10 ml to group S and 10ml NaCl 0.9% to group C. All BSCPB is performed by experienced anesthesia doctor after a standardized induction of general anaesthesia.eneral anaesthesia was induced by using intravenously with midazolam,propofol, fentanyl, cisatracurium is injected IV to facilitate orotracheal intubation. After a standardized induction of general anaesthesia, patients receive Regional Anesthesia at the discretion of the experienced anesthesiologist who was blinded to treatment.

The patient is placed in a supine position with the head turned away from the side to be blocked, and then the sternocleidomastoid muscle (SCM) is identified by slight head elevation. SCPB is performed with a 26-gauge needle that is inserted at the midpoint of the posterior border of the SCM muscle and the needle is advanced just past the SCM muscle.

Enrollment

79 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

-Eligible patients fit an ASA I or II classification adult patients who will be scheduled for elective thyroid lobectomy under general anaesthesia.

Exclusion criteria

  • hypersensitivity to any study drugs
  • Long-term use of anticoagulant drugs: warfarin or heparin
  • the neck or systemic infection
  • communication disorder
  • refuse to accept this research subjects.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

79 participants in 2 patient groups, including a placebo group

nerve block
Active Comparator group
Description:
cervical plexus block with ropivacaine
Treatment:
Procedure: nerve block
Placebo
Placebo Comparator group
Description:
placebo saline
Treatment:
Procedure: placebo

Trial contacts and locations

2

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Central trial contact

Xiangcai Ruan, MD,PHD; Yuan Lin, MD, Msc

Data sourced from clinicaltrials.gov

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