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Comparison of conscious sedation with dexmedetomidine or propofol for inguinal hernia repair: a prospective randomized controlled trial

Comparison of conscious sedation with dexmedetomidine or propofol for inguinal hernia repair: a prospective randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-15007086
Enrollment
Unknown
Registered
2015-09-22
Start date
2014-08-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

inguinal hernia

Interventions

1:propofol combination with fentanyl
2:dexmedetomidine combination with fentanyl

Sponsors

Zhejiang Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 80 adult patients between ages 18 70 years old, American Society of Anesthesiologists (ASA) physical status I-II, who underwent unilateral inguinal hernia repair.

Exclusion criteria

Exclusion criteria: Patients with chronic pain, history of opioid addiction, body mass index (BMI) above 40 kg/m2, those allergy to local anesthetics were excluded.

Design outcomes

Primary

MeasureTime frame
Postoperative pain score;Time for onset of sedation;Recovery time;Patient's satisfaction;The requirement of fentanyl;—

Secondary

MeasureTime frame
Mean arterial pressure;Heart rate;—

Countries

China

Contacts

Public ContactWang Hongmei
whm87783648@126.com+86 13858032079

Outcome results

None listed

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