Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 12:59 AM
Ignite Modification Date:
2025-12-25 @ 12:59 AM
NCT ID:
NCT00666393
Eligibility Criteria:
Inclusion Criteria:
* The patients must: weigh \>= 40 kg
* be scheduled for abdominal, pelvic/genitourinary, orthopedic, or thoracic surgery
* Be expected by the investigator's staff to require injected opioid analgesia for at least 24 hours after surgery
* Be judged by the investigator's staff to be capable of understanding and cooperating with the requirements of the study.
Exclusion Criteria:
* Patients who have undergone any surgery on the airway, head or neck
* Patients who are expected to require intensive care
* Patients who require airway(breathing) support after their surgery
* Patients who received intra-operative (during surgery) and/or post-operative (after surgery) administration of opioids other than morphine, hydromorphone, fentanyl, sufentanil or alfentanil
* Patients with active generalized skin disorders or active local skin disease that precludes the application of fentanyl iontophoretic transdermal system(40 mcg).
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
6 Years
Maximum Age:
17 Years
Study:
NCT00666393
Study Brief:
Protocol Section:
NCT00666393