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The EFFICIENCY of FASCIAL PLANE BLOCKS in BARIATRIC SURGERY

CAN POSTOPERATIVE PAIN BE PREVENTED in BARIATRIC SURGERY? EFFICACY and USABILITY of FASCIAL PLANE BLOCKS: a RETROSPECTIVE CLINICAL STUDY

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05284695
Enrollment
113
Registered
2022-03-17
Start date
2019-01-01
Completion date
2021-12-31
Last updated
2025-04-02

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

Conditions

Bariatric Surgery Candidate, Post Operative Pain, Regional Anesthesia Morbidity

Brief summary

Bariatric surgery effectively produces weight loss and reduces obesity-related comorbidities. Although it is mostly performed with minimally invasive techniques, the patients may still suffer from moderate-to-severe pain immediately after surgery \[1\]. Opioids remain the first choice for multimodal analgesia in the treatment of postoperative pain. Providing analgesia after bariatric surgery might be challenging due to a high prevalence of obstructive sleep apnea syndrome and the increased sensitivity to respiratory depression triggered by opioid overuse after surgeryThe most common plane block techniques utilized during laparoscopic bariatric surgery are transversus abdominis plane block (TAP), rectus sheath block (RB), the erector spinae plane block (ESPB) and the external oblique intercostal block (EOI). In this study, we have evaluated the auxiliary benefit of these various techniques in reduction of the postoperative in bariatric surgery. patients who had laparoscopic bariatric surgery at VKV American Hospital between January 2019 and December 2021 were reviewed retrospectively.

Interventions

PROCEDUREBariatric surgery

Patients undergoing elective bariatric surgery

Sponsors

V.K.V. American Hospital, Istanbul
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Patients undergoing elective bariatric surgery

Exclusion criteria

* Patients with a history of cerebrovascular events * Alzheimer's and dementia * inadequate cognitive functions * history of chronic pain * long-term opioid therapy

Design outcomes

Primary

MeasureTime frameDescription
postoperative analgesia0 - 24 hoursPostoperative pain assessment of patients will be made with a numeric rating scale (NRS). Postoperative opioid consumption will be examined

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026