Catheter-related bladder discomfort
Conditions
Interventions
Control group(C Group) Ropivacaine alone in sacral canal block group:Before general anesthesia induction, 0.35% ropivacaine 10 ml was given under ultrasound guided sacral canal block.
Trial group (I Group)Ropivacaine combined with dexmedetomidine in sacral canal block group:Before general anesthesia induction, 10 ml of dexmedetomidine1ug/kg and 0.35% ropivacaine were given under ul
Sponsors
Beijing Miyun District Hospital
Eligibility
Sex/Gender
Male
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1.ASA ?or ? grade; 2.Age 18 years or older; 3.Male patients with indwelling catheters after anesthesia; 4.Ureteroscopic lithotripsy under elective general anesthesia;
Exclusion criteria
Exclusion criteria: 1.Long-term use of anticoagulants for coagulation dysfunction, associated with neuromuscular diseases or sensory disorders,sacral canal block contraindications. 2.Mental disorders,cognitive disorders; 3.History of abnormal urethral morphology; 4.Urinary tract infection and urinary tract irritation; 5.Bladder dysfunction such as excessive bladder syndrome,neurogenic bladder dysfunction; 6.Benign Prostatic Hyperplasia; 7.History of narcotic analgesic drug dependence; 8.Refusing or unable to cooperate;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of catheter-related bladder discomfort 24 hours after surgery; | — |
Secondary
| Measure | Time frame |
|---|---|
| The occurrence of delirium;Bromage score;Agitation score;Nausea and vomiting;The use of remedial analgesics for postoperative catheter-related bladder discomfort pain;Catheter-related bladder discomfort severity rating;Ramsay sedation score;Visual analogue score(VAS);Sleep score;Duration of analgesia; | — |
Countries
China
Contacts
Public ContactShao Lina
Beijing Miyun District Hospital
Outcome results
None listed