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Postoperative urinary retention in orthopedic patients

Acute postoperative urinary retention in orthopedic patients undergoing Spinal Anesthesia with Morphine versus Spinal Anesthesia without opioid associated with Peripheral Nerve Block: a randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-9rhyjn
Enrollment
Unknown
Registered
2020-03-08
Start date
2017-07-23
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Urinary retention

Interventions

Intervention: 26 patients in the BSA-Block group received subarachnoid anesthesia with 20 mg of Hyperbaric Bupivacaine and peripheral nerve block with 0.2 to 0.375% Ropivacaine, in a volume of 20 to 3
Procedure/surgery

Sponsors

Carolina Lourenzon Schiavo
Lead Sponsor
Hospital de Clinicas de Porto Alegre
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Patients over 18 years of age; undergoing elective orthopedic surgeries of the lower limbs at the Hospital de Clinicas de Porto Alegre; with acceptance and signature of the free and informed consent term; with the possibility of performing the surgical procedure under spinal anesthesia; a minimum hospital stay forecast of 24 hours.

Exclusion criteria

Exclusion criteria: Patients with a history of urological problems; severe cognitive disorders; patients who were unable to urinate spontaneously before surgery.

Design outcomes

Primary

MeasureTime frame
Evaluate the incidence of urinary retention in both groups, as verified by the need for urinary catheterization and the time required until the first spontaneous urination

Secondary

MeasureTime frame
Assess the incidence of nausea and vomiting within 24 hours;Evaluation of postoperative pain in both groups in 12 and 24 hours. Evaluation performed using the visual analog scale of pain;Evaluate the consumption of opioids (morphine and codeine), verified by the dose used by each patient in 24 hours

Countries

Brazil

Contacts

Public ContactCarolina ;Carolina Schiavo;Schiavo

Hospital de Clinicas de Porto Alegre;Hospital de Clinicas de Porto Alegre

carolinaschiavo@yahoo.com;carolinaschiavo@yahoo.com+55 51 33598226;51 3359 8226

Outcome results

None listed

Source: REBEC (via WHO ICTRP)