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Effects of nefopam on catheter-related bladder discomfort

Effects of preemptive nefopam administration on postoperative catheter-related bladder discomfort in urogenital surgery under spinal anesthesia : A prospective, randomized, double-blind study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0002758
Enrollment
54
Registered
2018-03-28
Start date
2017-01-05
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

None listed

Interventions

Drug : The randomization was done by a computer-generated random numbers on surgery day.Before induction of spinal anesthesia, patients belonging to Group P received 100 ml of normal saline as placebo

Sponsors

Kyungpook National University Medical Center
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: Adult patients aged 20 to 75 years who were American Society of Anesthesiologists (ASA) physical status I or II of male, undergoing transurethral resection of bladder.

Exclusion criteria

Exclusion criteria: A. patients who had known allergic to any medicines B. patients who had a history of drug or alcohol abuse C. patients who had chronic pain D. patients who had taken analgesics within 24 hours before surgery E. patients who had history of taking nefopam

Design outcomes

Primary

MeasureTime frame
incidence and severity of catheter related bladder discomfort

Secondary

MeasureTime frame
pain, Numeric rating score , NRS, 0=no pain, 10=the worst pain;side effects (nausea/vomoting, tachycardia, dizziness, drowsiness, sweating);the effects of nefopam on spinal anesthesia, the time of maximum sensory block, the time of 2 segments regression

Countries

Korea, Republic of

Contacts

Public ContactKyung-Hwa Gwak

Kyungpook National University Medical Center

kwakkh@hotmail.com+82-53-200-5862

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026