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LigaSure Small Jaw® Versus Conventional Neck Dissection in Head and Neck Cancer Patients

Phase 4
Completed
Conditions
Head and Neck Neoplasms
Interventions
Procedure: Neck dissection
Registration Number
NCT02597582
Lead Sponsor
Taichung Veterans General Hospital
Brief Summary

The aim of this prospective randomized study was to investigate if the LigaSure vessel sealing system can reduce the operation duration and the postoperative drainage amount in patients undergoing neck dissection.

Detailed Description

We compared the differences in perioperative and postoperative variables between LigaSure Small Jaw®-assisted and conventional neck dissection in head and neck cancer patients.

Patients who were scheduled to undergo neck dissection due to head and neck cancer were eligible for this study. After receiving a detailed explanation, all patients signed an informed consent form before randomization. The study group were treated using the LigaSure vessel sealing system (Small Jaw®; Covidien, Colorado, USA) for dissection and hemostasis throughout the whole procedures during neck dissection. Relevant data included tumor-related variables, perioperative parameters, postoperative drainage status, postoperative subjective pain, and analgesic consumption amount were recorded and analyzed.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
41
Inclusion Criteria
  • Patients aged 20 to 80 years scheduled to receive neck dissection due to head and neck cancer
Exclusion Criteria
  • history of coagulation disorders
  • prior radiation to the neck
  • prior neck dissection
  • declined to participate

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Conventional neck dissectionNeck dissectionThe control group patients were treated using conventional cold instrument dissection, monopolar electrocautery hemostasis, and suture ligation during neck dissection. Participants were asked to take a Voren enteric-microencapsulated (Diclofenac 50 mg/capsule) capsule 3 times a day for pain relief postoperatively. An additional capsule before sleep was allowed if persistent pain was told by the patient. When intolerable pain was complained in spite of oral analgesic, pethidine (meperidine 50 mg/ampule) injection was prescribed every 6 hours.
Ligusure assisted neck dissectionNeck dissectionThe study group patients were treated using the LigaSure vessel sealing system (Small Jaw® with ForceTriad®; Covidien, Colorado, USA) for dissection and hemostasis throughout the whole procedures during neck dissection. Participants were asked to take a Voren enteric-microencapsulated (Diclofenac 50 mg/capsule) capsule 3 times a day for pain relief postoperatively. An additional capsule before sleep was allowed if persistent pain was told by the patient. When intolerable pain was complained in spite of oral analgesic, pethidine (meperidine 50 mg/ampule) injection was prescribed every 6 hours.
Primary Outcome Measures
NameTimeMethod
Opreation Duration1 day

The duration from incision of cervial skin till the completion of lymph node dissection

Secondary Outcome Measures
NameTimeMethod
Postoperative Oral Analgesic Consumption2 weeks

The amount of analgesic consumption via oral ingestion after operation

Intraoperative Blood Loss1 day

Intraoperative blood loss was estimated by the sum of the volume in the suction bottle and the increased weight of wet gauzes containing blood after neck dissection.

Postoperative Subjective Pain Status2 weeks

Visual analogue scale of subjective pain status after operation

Postoperative Injected Analgesic Amount2 weeks

The amount of injected form analgesic used (Meperidine 50 mg/ampule)

Postoperative Drainage Amount2 weeks

The amount of drainage from closed system drainage tube

Trial Locations

Locations (1)

Taichung Veterans General Hospital

🇨🇳

Taichung, Taiwan

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