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NCT07346599
A Block Method for Pain After Back Surgery
NA trial testing ESP block group in Nerve Block in 102 participants. Completed in 20 May 2022.
20 May 2022
Quick facts
| Lead sponsor | Kutahya City Hospital |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | supportive care |
| Enrollment | 102 |
| Start date | 27 September 2021 |
| Primary completion | 20 May 2022 |
| Estimated completion | 20 May 2022 |
| Sites | 1 location across Turkey (Türkiye) |
Drugs / interventions tested
- ESP block group
Conditions studied
- Nerve Block — all drugs for Nerve Block →
- Postoperative Pain — all drugs for Postoperative Pain →
- Randomised Clinical Trial — all drugs for Randomised Clinical Trial →
Sponsor
Kutahya City Hospital
Who can join
Adults 18 to 80, any sex, with Nerve Block or Postoperative Pain. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The purpose of this clinical trial is to evaluate whether bilateral lumbar erector spinae plane (ESP) block can reduce postoperative pain in adult patients undergoing lumbar spine surgery. The study also assesses the safety of this method and its effects on the recovery process. The main questions it aims to answer are: Do patients who receive the ESP block experience less postoperative pain? Do these patients require fewer opioid (morphine-derived) analgesics? Does the first analgesic requirement occur later? Do patients mobilize earlier (stand/walk sooner)? Does the ESP block affect hemodynamic stability during and after surgery? Researchers will compare the ESP block group with the standard analgesia group to determine whether these effects occur. Participants: Patients in this study will be asked to: Be randomly assigned to one of two groups before lumbar spine surgery Receive either a bilateral ESP block or standard analgesic therapy Undergo postoperative follow-up including: measurement of pain scores, recording of analgesic consumption, assessment of time to first analgesic requirement, monitoring of mobilization time, valuation of possible side effects
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT07346599
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of ESP block group
Trials testing the same drug.
- NCT07011069 — Rhomboid Intercostal and Subserratus Plane Block vs Erector Spinae Plane Block in Video-Assisted Thoracoscopic Surgery · NA · recruiting
- NCT06419504 — The Effect of Ultrasonography-guided Fascial Plane Blocks in Breast Cancer Surgery Patients · completed
- NCT06660966 — Comparison Of M-TAPA Block and ESP Block İn Laparoscopic Cholesystektomy · NA · completed
- NCT04189289 — Laparoscopic Bariatric Surgery and Erector Spinae Plane Block · NA · completed
- NCT03619447 — Comparison of ESP Block Versus Serratus Block · Phase 4 · unknown
Other recruiting trials for Nerve Block
Currently open trials in the same condition.
- NCT07509866 — Liposomal Bupivacaine Versus Ropivacaine With Perineural Dexamethasone or Dexmedetomidine as Adjuncts for Adductor Canal · NA · recruiting
- NCT07346885 — Lumbar-Sacral Plexus Block vs Fascia Iliaca Block Plus Low-Dose Spinal Anesthesia for Femoral Neck Fracture Surgery · NA · active not recruiting
- NCT07249827 — A Randomized Comparison Between 0.67 mcg/kg, 1 mcg/kg, and 1.33 mcg/kg of Perineural Dexmedetomidine for Ultrasound-Guid · Phase 2 · recruiting
- NCT07239817 — PENG Block + LIA For Endoprosthesis Surgery With Anterior Approach · NA · recruiting
- NCT07510269 — Investigation of the Effects of Serratus Posterior Superior Intercostal Plane Block and Serratus Anterior Plane Block on · NA · recruiting
Other Kutahya City Hospital trials
Trials by the same sponsor.
- NCT06862232 — P : Ingrown Toenail Patient I : Bird Flap Surgery C : Noel Winograd Method O : Recurrence, Complications, Functional Out · NA · not yet recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT07346599 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Kutahya City Hospital
- Last refreshed: 16 January 2026
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07346599.
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