Pain relief after surgery for patients undergoing kidney stone removal

COMPARISON OF ULTRASOUND GUIDED ERECTOR SPINAE BLOCK AND FLUOROSCOPY GUIDED PERITUBULAR INFILTRATION FOR POST OPERATIVE ANALGESIA IN PERCUTANEOUS NEPHROLITHOTOMY PATIENTS- A RANDOMIZED DOUBLE BLINDED CLINICAL TRIAL

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2022/01/039865

Enrollment

Registered

2022-01-31

Start date

Unknown

Completion date

Unknown

Last updated

2022-02-21

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

Conditions

Health Condition 1: N200- Calculus of kidney

Interventions

Intervention1: Erector Spinae Block: Erector Spinae Block will be given on surgery side at T11 Level with Inj.Bupivacaine 0.25% 20ml, after surgery before extubation and will be observed for 24 hours

Eligibility

Inclusion criteria

Inclusion criteria: ASA physical status I â?? IV Age 18 years and above Patient undergoing Unilateral Single puncture Percutaneous Nephrolithotomy

Exclusion criteria

Exclusion criteria: Contraindications for local anesthetics Duration of procedure >3hrs Multiple punctures Excessive bleeding Inability to comprehend Verbal Numeric Rating Scale (VNRS) BMI >30 kg/m2

Design outcomes

Primary

Measure	Time frame
To compare the efficacy of USG-ESPB, FG-PI and Control by assessing total 24hr mean Inj.Tramadol consumption in 3 groups.Timepoint: 24 hour assessment of pain scores at 4th hourly after intervention/ surgery and administration of Inj.Tramadol according to pain scores	—

Secondary

Measure	Time frame
To assess the quality of Static and Dynamic pain relief by Verbal Numeric Rating ScaleTimepoint: Static and dynamic Score every 4 th hourly for 24 hours;To compare duration of AnalgesiaTimepoint: the time taken to recieve rescue analgesia - injection tramadol after procedure in all three groups;To observe and record complications such as Nausea, Vomiting and SedationTimepoint: for knowing side effects for the intervention;To record and access Patient Satisfaction about the pain relief.Timepoint: For knowing patient preferrance and satisfaction for the intervention;To record Hemodynamic Parameters â?? HR, BP (SBP, DBP, MAP), RR, SPO2 every 4th hourly till 24hrTimepoint: to observe any significant change in parameters after intervention	—

Measure

Time frame

To assess the quality of Static and Dynamic pain relief by Verbal Numeric Rating ScaleTimepoint: Static and dynamic Score every 4 th hourly for 24 hours;To compare duration of AnalgesiaTimepoint: the time taken to recieve rescue analgesia - injection tramadol after procedure in all three groups;To observe and record complications such as Nausea, Vomiting and SedationTimepoint: for knowing side effects for the intervention;To record and access Patient Satisfaction about the pain relief.Timepoint: For knowing patient preferrance and satisfaction for the intervention;To record Hemodynamic Parameters â?? HR, BP (SBP, DBP, MAP), RR, SPO2 every 4th hourly till 24hrTimepoint: to observe any significant change in parameters after intervention

—

Countries

India

Contacts

Public ContactAntony John Charles S

Mahatma Gandhi Medical College and Research and Institute, Pondicherry

101anjukachu@gmail.com9497659887

Outcome results

None listed

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