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Postoperative Sleep Quality of Patients Anesthesia With Propofol or Sevoflurane Undergoing Thyroidectomy

C

China Medical University, China

Status and phase

Completed
Phase 4

Conditions

Postoperative Sleep Quality

Treatments

Drug: propofol
Drug: sevoflurane

Study type

Interventional

Funder types

Other

Identifiers

NCT02146976
20140522

Details and patient eligibility

About

The investigators designed a study to determine whether Propofol or Sevoflurane would provide same postoperative sleep quality in patients undergoing thyroidectomy.

Full description

The investigators designed a study to determine whether Propofol or Sevoflurane would provide same postoperative sleep quality in patients undergoing thyroidectomy.The bispectral index score (BIS) was monitored during the operation and the first postoperative night.

Enrollment

124 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Participants were deemed eligible if they were candidates for general anesthesia undergoing thyroidectomy

Exclusion criteria

  • Patients were excluded if they had a body mass index exceeding 30 kg/m2, had a Pittsburgh Sleep Quality Index global scores higher than 6, had an anesthesia time longer than 4 hours, had a history of cardiovascular, neurological, or psychiatric disease, had cervical lymph node metastasis, were treated with sedative and analgesics during the postoperative BIS-Vista monitoring period, were allergic to drugs used in the study, or had been diagnosed with Graves' disease or hyperthyroidism or hypothyroidism.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

124 participants in 2 patient groups

Propofol
Experimental group
Description:
introvenious infusion of propofol
Treatment:
Drug: propofol
Inhaled anaesthetic (Sevoflurane)
Experimental group
Description:
sevoflurane (1.0-1.3% Minimum Alveolar Concentration)
Treatment:
Drug: sevoflurane

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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