Obturator Block in Lateral Tumors of the Bladder: Does it Have Adverse Effects on Early Postoperative Mobilization?

• Sponsor: Ankara City Hospital Bilkent (Other)
• Overall Status: Not yet recruiting
• CT.gov ID: NCT05652309
• Collaborator: (none)
• Enrollment: 70
• Location: 1
• Anticipated Duration (Months): 11
• Patients Per Site Per Month: 6.4

Study Details

Study Description

Brief Summary

Investigation of delay in postoperative mobilization due to motor block and complications related to block in patients who underwent USG-assisted obturator nerve block with distal approach

Condition or Disease	Intervention/Treatment	Phase
Obturator Nerve Block; Ultrasound Guided Nerve Block; Complications Neurological	Procedure: spinal block and obturator nerve block

Study Design

• Study Type: Observational [Patient Registry]
• Anticipated Enrollment: 70 participants
• Observational Model: Cohort
• Time Perspective: Prospective
• Official Title: Obturator Block in Lateral Tumors of the Bladder: Does it Have Adverse Effects on Early Postoperative Mobilization?
• Anticipated Study Start Date: Jan 1, 2023
• Anticipated Primary Completion Date: May 1, 2023
• Anticipated Study Completion Date: Dec 1, 2023

Arms and Interventions

Arm	Intervention/Treatment
spinal anesthesia spinal block will be performed to patients after monitoring	Procedure: spinal block and obturator nerve block; spinal block and obturator nerve block
spinal anesthesia and obturator nerve block spinal block will be performed to patients after monitoring, and then the patients in the ONB block group will be given the appropriate position, with a USG-assisted distal approach, 5 cc %2 prilocain into the anterior and 5cc %2 prilocain into the posterior branch of the obturator nerve.	Procedure: spinal block and obturator nerve block; spinal block and obturator nerve block

Outcome Measures

Primary Outcome Measures

1. pin prick test [postoperatively 2nd hour]

   postoperatively sensation block

2. bromage score [postoperatively 2nd hour]

   motorial block

3. pin prick test [postoperatively 5th hour]

   postoperatively sensation block

4. bromage score [postoperatively 5th hour]

   motorial block

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years to 75 Years
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Inclusion Criteria:

• age between 18-75

• ASA1, ASA2, ASA 3 physical status

Exclusion Criteria:

1. The patient's refusal

2. Active infection in the area to be blocked

3. Kidney failure

4. Liver failure

5. Heart failure

6. BMI less than 18 and a BMI greater than 40

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Serap Diker	Ankara	Çankaya	Turkey

Sponsors and Collaborators

• Ankara City Hospital Bilkent

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Serap Diker, Anesthesiology and Reanimation, Ankara City Hospital Bilkent
• ClinicalTrials.gov Identifier: NCT05652309
• Other Study ID Numbers: E2-22-1854
• First Posted: Dec 15, 2022
• Last Update Posted: Dec 15, 2022
• Last Verified: Dec 1, 2022

• Individual Participant Data (IPD) Sharing Statement: Undecided
• Plan to Share IPD: Undecided
• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Additional relevant MeSH terms: Urinary Bladder Neoplasms

Study Results

No Results Posted as of Dec 15, 2022