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Preemptive Analgesia With Morphine Sulphate in Major Urological Surgery

Influence of Premedication With Oral Morphine Sulphate on Analgesic Consumption in Patient Undergoing Major Urological Surgery. Comparison Between Two Different Doses

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02041988
Enrollment
40
Registered
2014-01-22
Start date
2013-02-28
Completion date
2014-07-31
Last updated
2014-01-22

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

Conditions

Pain

Keywords

premedication, oral morphine, preemptive analgesia

Brief summary

In this study safety and efficacy of oral morphine sulphate is evaluated in order to reduce opioids administration during major urological surgery

Detailed description

The administration of oral morphine sulfate could be useful to reduce the use of opioids in major urological surgery. This study aims to assess the safety and efficacy of two different oral morphine sulphate doses 0,2 mg/kg vs 0,4mg/kg in major urological surgery.

Interventions

None listed

Sponsors

University of Roma La Sapienza
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

American Society of Anaesthesiologists physical status classification I/ II, age between 18 - 75, BMI 18 -30

Exclusion criteria

American Society of Anaesthesiologists physical status classification III/ IV, renal and hepatic insufficiency, postoperative nausea and vomiting after oral opioids administrations, neurological and psychiatric disorders.

Design outcomes

Primary

MeasureTime frame
morphine sulphate consumptionsix months

Secondary

MeasureTime frame
vital signssix months

Other

MeasureTime frame
VAS scoresix months
side effectssix months

Countries

Italy

Contacts

Primary ContactFrancesco FC Cannata, MD
francesco.cannata@uniroma1.it+390649970283

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026