A Bridging Trial Comparing Sugammadex (Org 25969) at Reappearance of T2 in Japanese and Caucasian Participants. Part A: Japanese Participants (P05956)

• Status: Completed
• Trial end date: 2006-12-18
• Target enrollment: 0
• Participant gender: All

Summary

The objective of this trial was to establish the dose-response of T2 (the amplitude of the first response of second twitch to train of four (TOF) stimulation, expressed as percentage of control first twitch,T1) in Japanese and Caucasian participants. Part A: Japanese Participants

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Merck Sharp & Dohme Corp.
• Treatments: Rocuronium; Vecuronium Bromide

Criteria

Inclusion Criteria:

• Is of American Society of Anesthesiologists (ASA) class 1 - 3;

• Is at least 20 years but under 65 years of age;

• Japanese participants;

• Is scheduled for elective surgery in supine position and under sevoflurane anesthesia, in need of administration of neuromuscular blocking agents (NMBAs), with an anticipated duration of about 1.5-3 hours;

• Has given written informed consent.

Exclusion Criteria:

• Participants in whom a difficult intubation because of anatomical malformations was expected;

• Is known or suspected to have neuromuscular disorders impairing the effect of NMBAs and/or significant renal dysfunction (for example a creatinine level > 1.6 mg/dl) and/or severe hepatic dysfunction.

• Is known or suspected to have a (family) history of malignant hyperthermia;

• Is known or suspected to have an allergy to narcotics, muscle relaxants or other medication used during general anesthesia;

• Is receiving medication expected to interfere with the rocuronium or vecuronium given in this trial, based on the dose and time of administration;

• Females who were pregnant;

• Females not using birth control or using only oral contraception as birth control continuously;

• Were breast-feeding;

• Has already participated in P05956, or in another trial with sugammadex;

• Has participated in another clinical trial within 6 months of entering into P05956