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Abdominal wall block decrease intraoperative opioid consumption using surgical pleth index-guided remifentanil administration in single-port laparoscopic herniorrhaphy

Abdominal wall block decrease intraoperative opioid consumption using surgical pleth index-guided remifentanil administration in single-port laparoscopic herniorrhaphy; a prospective randomized controlled trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0002813
Enrollment
64
Registered
2018-04-21
Start date
2018-04-16
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

None listed

Interventions

Procedure/Surgery : Remifentanil continuous infusion using surgical pain index At the beginning of general anesthesia, anesthesiologists prepare a syringe pump with target controlled infusion (TCI).
in total 60 ml. All block will be done with ultrasound guided. Use 40 ml of the mixture to block the house (20 ml each on each side) and use 20 ml to block the waist square.

Sponsors

The Catholic University of Korea, Daejeon St. Mary's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: slingle port laparoscoic surgery ASA classiffication score 3point or less

Exclusion criteria

Exclusion criteria: The American Society of Anesthesiologists 4 point or more Patients with chronic pain syndrome, patients with a history of drug dependence, Those who can not communicate with researchers, Patients who have received anticoagulants or bleeding disorders. If the BMI exceeds 35, Patients with antihypertensive drugs or arrhythmia Those who require or refuse neuroprotection

Design outcomes

Primary

MeasureTime frame
The amount of remifentanil (ng / kg / min) from the start of surgery (incision) to the end of surgery (wound closure)

Secondary

MeasureTime frame
Additional painkillers and anti-emetic agents;total SPI score;The time related to recovery (spontaneous breathing, eye opening, time to extubation, time from recovery room to discarge)

Countries

Korea, Republic of

Contacts

Public ContactWOOJIN KWON

The Catholic University of Korea, Daejeon St. Mary's Hospital

ktuttle8150@gmail.com+82-42-220-9046

Outcome results

None listed

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