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Effect Of Intravesical Alkalinized Lidocaine solution as Local Anesthesia Prior to Cystoscopy on Post-Operative Pain Scores

Effect Of Intravesical Alkalinized Lidocaine solution plus Lidocaine Gel Versus Lidocaine Gel alone as Local Anesthesia Prior to Cystoscopy on Post-Operative Pain Scores: A Prospective, Single Centre, Randomized, Double-Blind, Parallel Group Trial of Efficacy and Morbidity - Nil

Status
Recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/067828
Enrollment
154
Registered
2024-05-24
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Health Condition 1: N329- Bladder disorder, unspecified Health Condition 2: N329- Bladder disorder, unspecified Health Condition 3: N399- Disorder of urinary system, unspecified Health Condition 4: O- Medical and Surgical

Interventions

Intervention1: AL group(Alkalinised Lignocaine+Lidocaine gel): Group A (AL group): In this group, patients will receive 10 ml of Lidocaine gel. 30 ml of the Alkalinised Lignocaine (AL) solution (Alkal

Sponsors

All India Institute of Medical Sciences Bhubaneswar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients aged 18 years or above undergoing cystoscopy(CPE) for following conditions- Check cystoscopy in Ca bladder patients in follow up, CPE for LUTS under evaluation and CPE for hematuria under evaluation 2. Written informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients not giving consent. 2. Neurological disease that may affect bladder function/sensation (mainly MS). 3. Serious concomitant illness. 4. Patients with known drug allergy to local anesthetic drugs. 5. Patients with severe cardiovascular compromise.

Design outcomes

Primary

MeasureTime frame
To compare pain scores (100 mm Visual Analogue Scale score) amongst patients undergoing cystoscopy under Intravesical alkalinised lidocaine solution plus Lidocaine gel vs Lidocaine gel alone.Timepoint: 0 hour AND 1 hour

Secondary

MeasureTime frame
b) To compare the incidence of UTI- The participant will be contacted 1 week after and asked about symptoms of UTI: Dysuria, cloudy urine, pollakiuria, nocturia.Timepoint: 1 week;To compare patient tolerance as assessed by surgeon on 100 mm Visual Analogue Scale score.Timepoint: 0 hour;To compare postoperative complications: voiding difficulty and hematuria.Timepoint: 0 hour, 1 hour and 1 week;To compare the participant experience with the procedureTimepoint: 1 week

Countries

India

Contacts

Public ContactKirti Singh

AIIMS, Bhubaneswar

kirtisingh2604@gmail.com9532682693

Outcome results

None listed

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