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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00504283
Other study ID # CPHS 20569
Secondary ID
Status Completed
Phase N/A
First received July 17, 2007
Last updated October 17, 2007
Start date February 2007
Est. completion date October 2007

Study information

Verified date October 2007
Source Dartmouth-Hitchcock Medical Center
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

An analgesia protocol for acute renal colic will lead to faster significant reductions in pain than prior practice.


Description:

A retrospective study was performed that assessed the time to significant analgesia and medications used to achieve analgesia in the DHMC ED. Based upon this a prospective pain management protocol was designed and we will track the difference in time to significant pain relief between the two groups.


Recruitment information / eligibility

Status Completed
Enrollment 45
Est. completion date October 2007
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Kidney stone on stone protocol CT scan

- Acute pain from a kidney stone

Exclusion Criteria:

- Age < 18 or > 65

- Pregnant women

- Contraindications to NSAID's or opiates

Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Intervention

Drug:
Toradol

Morphine


Locations

Country Name City State
United States DHMC Lebanon New Hampshire

Sponsors (1)

Lead Sponsor Collaborator
Dartmouth-Hitchcock Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Time to significant pain relief Within emergency department
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