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OpenTrials
Completed

NCT Number: NCT02680353

The Perioperative Analgesic Efficiency of Bilateral Superficial Cervical Plexus Block in Patients With Thyroidectomy

To determine the postoperative analgesic efficiency of bilateral superficial plexus block, patients are divided into two groups. Study group received bilateral superficial plexus block, where control had none. Visual analog scale, opioid consumption and presence of nausea-vomiting are recorded.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Gaziosmanpasa University

Tokat Province, 60200, Turkey (Türkiye)

About this study

Bilateral superficial cervical plexus block has successfully been demonstrated to provide an efficient analgesia in patients with thyroidectomy, parathyroidectomy, carotis end-arterectomy. The present study is aimed to investigate the intraoperative hemodynamic responses, anesthetic and analgesic consumption, and postoperative recovery quality of bilateral superficial cervical plexus block in patients with total thyroidectomy. After approval, patients enrolled in the study is invited to complete the Pain Catastrophizing Scale questionnaire. Patients are divided into two groups by computer-based randomization technique as control and study group. After standard monitorization, anesthesia induction and tracheal intubation, bilateral superficial cervical plexus block is performed to study group and no intervention to control group. At the end of the operation all patients received paracetamol 1 gr intravenous. In postoperative period, visual analog scale values, opioid consumption, presence of nausea-vomiting, anti-emetic usage or any other complications are recorded.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Over 18 years of age
  • Planned to undergo thyroidectomy
  • An American Society of Anesthesiologists score of 1 or 2

Exclusion criteria

  • Severe cardiovascular disease
  • Psychiatric diseases
  • Difficult intubation
  • Rejected to participation

Treatment and study plan

Bilateral superficial cervical plexus block

Procedure

A kind of anesthetic nerve block type performed to block the nerve function temporarily by administrating local anesthetics through the trajectory of the nerve.

Primary outcomes

  1. Visual analog scale

    Time frame: one time in postoperative period for one year

Secondary outcomes

  1. Presence of nausea-vomiting

    Time frame: In postoperative period for one year

  2. Mean arterial pressure

    Time frame: In both intraoperative and postoperative period for one year

  3. Heart rate

    Time frame: In both intraoperative and postoperative period for one year

  4. Antiemetic usage

    Time frame: postoperative period for one year

  5. respiratory rate

    Time frame: postoperative period for one year

  6. opioid consumption

    Time frame: During postoperative period for one year

Sponsors and collaborators

Lead sponsor

Tokat Gaziosmanpasa University

Other

Registry information

Important dates

Study start
2015
Primary completion
2016
Study completion
2016
First posted
Feb 11, 2016
Registry last updated
Apr 19, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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