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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00385541
Other study ID # AAAA2949
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date November 2003
Est. completion date October 2007

Study information

Verified date July 2018
Source Columbia University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Both morphine and hydromorphone are pain medications commonly used after surgery. It is thought at the institution that hydromorphone causes less side effects but this has not been studied. The study proposes to treat the patients with either morphine or hydromorphone and determine how much nausea, vomiting, and itching they have with each drug


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date October 2007
Est. primary completion date October 2007
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- patients scheduled for abdominal surgery requiring post-operative PCA

- ASA = I or II

Exclusion Criteria:

- preoperative pain or use of pain medication

- narcotic allergy

- morbid obesity (Body Mass Index > 30)

- diagnosis of sleep apnea

- hepatic or renal disease

- use of medications that would affect narcotic pharmacodynamics

- preoperative nausea, vomiting, or pruritis

- diagnosis of alcoholism

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Morphine PCA
Morphine 1mg/mL, dose 1mL, lockout 6 minutes, max 10mL
Hydromorphone PCA
hydromorphone PCA 0.2mg/lml, dose 1ml, lockout 6min, max 10ml

Locations

Country Name City State
United States Columbia Presbyterian Hospital New York New York

Sponsors (1)

Lead Sponsor Collaborator
Columbia University

Country where clinical trial is conducted

United States, 

References & Publications (1)

Hong D, Flood P, Diaz G. The side effects of morphine and hydromorphone patient-controlled analgesia. Anesth Analg. 2008 Oct;107(4):1384-9. doi: 10.1213/ane.0b013e3181823efb. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Nausea Assessment by Patient Nausea scale range: (0 = none, 10 = the worst), ordinal. 1 hour after surgery, 8 hours after surgery
Secondary Mean Score on the Numeric Rating Scare (NRS) Pruritus Scale The NRS Pruritus Scale was used to measure magnitude of pruritus (0 = none, 10 = the worst). 1 hour after surgery, 8 hours after surgery
Secondary Pain Assessment by Patient Numeric Rating Scale for Pain: (0 = none, 10 = the worst), ordinal. 1 hour after surgery, 8 hours after surgery
Secondary The Number of Patients Who Vomited 1 hour after surgery, 8 hours after surgery
Secondary Mean Score on the Ramsey Scale of Sedation The Ramsey scale is used as a measure of sedation from 1 (the patient in anxious and agitated) to 6 (the patient exhibits no response). 1 hour after surgery, 8 hours after surgery
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