NCT06728514CompletedPhase 2/3
Comparative Study of USG Guided ESPB vs USG Guided PVB For Post-op Analgesia In Patient's After Open Renal Surgeries
Comparative Study of Ultrasound Guided Erector Spinae Plane Block vs Ultrasound Guided Paravertebral Block For Post-oprative Analgesia In Patient's After Open Renal Surgeries
Source: ClinicalTrials.gov · Last updated 4 May 2026
Brief summary (registry, in English)
Pain control following open renal surgeries are of utmost importance in order to reduce the chance of chronic pain development, and facilitate early rehabilitation. The erector spinae plane block (ESPB) is a recently developed regional anaesthesia procedure successfully used for different types of surgical procedures including open renal surgeries. A Comparative cross-sectional study design will be used and patients fulfilling the inclusion criteria will be included that are admitted through the Outpatient department. Patients will be optimized for surgery. A detailed history will be taken regarding the mode of injury, any preexisting disease and previous surgery and finally thorough examination of the patient will be done to rule out any systemic disease. Informed consent will be taken. These patients will be divided into 2 groups by simple lottery method in group A and B.All the data collected will be entered and analyzed by SPSS version 25.0. Age, surgery d.uration, intraoperative heart rate, intraoperative MAP, total postoperative opioid consumption, total intraoperative opiod and isoflurane consumption, time to first required analgesic, and VAS during the first postoperative 24 h will be summarized, according to normality, into mean (± standard deviation \[SD\]) or median (range). According to data normality, the hypothesis of significant differences between the two studied groups will be challenged using the one-way analysis of variance (with least significant difference correction) or Kruskal-Wallis tests (VAS). Moreover, a p value of \< 0.05 will be regarded to be statistically significant
- Status (registry)
- Completed
- Phase (registry)
- Phase 2/3
- Study type
- Interventional
- Enrollment
- 72 (actual)
- First submitted
- 29 Sept 2024
- Start date
- 11 Jan 2024
- Primary completion date
- 9 Jul 2024
- Lead sponsor
- Sahiwal medical college sahiwal
- Diseases
- High blood pressure
- NCT number
- NCT06728514
What you commit to
- Study type: Interventional · Phase 2/3
- Participants enrolled: 72
- From 11 Jan 2024 to the primary completion date, 9 Jul 2024
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Alcohol or drug abuse.
- Taking of pain medications within 24 h before surgery.
Other illness
- Relevant drug allergy.
- Infection at the site of injection.
- Chronic hepatic or renal failure.
Other
- Patients who do not give consent.
- Pregnancy
- Deranged coagulation profile
Who the study is looking for
- Both Genders
- Age between 18 years to 60 years.
- BMI ≤ 30 kg/m2
- ASA I or ASA II
Age in the registry: 18 years to 60 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Sahiwal Medical College,Sahiwal Coordinator of this site? Confirm its status | Sahiwal | Pakistan | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.