Quadratus Lumborum Block by Paraspinous Sagittal Shift Approach for Hip Surgery
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| ClinicalTrials.gov Identifier: NCT04628923 |
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Recruitment Status :
Not yet recruiting
First Posted : November 16, 2020
Last Update Posted : November 16, 2020
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Self Efficacy | Other: QUADRATUS LUMBORUM BLOCK | Phase 3 |
| Study Type : | Interventional (Clinical Trial) |
| Estimated Enrollment : | 5 participants |
| Allocation: | N/A |
| Intervention Model: | Single Group Assignment |
| Masking: | None (Open Label) |
| Primary Purpose: | Supportive Care |
| Official Title: | Tthe Anaesthetic Efficacy of Quadratus Lumborum Block by Paraspinous Sagittal Shift Approach for Hip Surgery:a Case Series |
| Estimated Study Start Date : | November 20, 2020 |
| Estimated Primary Completion Date : | December 30, 2020 |
| Estimated Study Completion Date : | December 30, 2020 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: QLB
With the patient in the lateral decubitus and the block side independent, a curvilinear ultrasound transducer (2-5 MHz) will be directed caudally in a sagittal plane 3-4 cm lateral to the lumbar spinous process of L4, which is almost opposite to the iliac crest, producing a longitudinal scan of the lumbar paravertebral region; and thus identifying the transverse processes of L3 and L4, with PM muscle in-between and erector spinae muscle posteriorly. The probe is shifted slowly to the lateral side until the transverse processes disappear and the QL muscle is evident in its long axis attached caudally to the iliac crest with a characteristic sonographic image of three muscle layers appearing from posterior to anterior as: erector spinae, QL, and PM muscles respectively. |
Other: QUADRATUS LUMBORUM BLOCK
QUADRATUS LUMBORUM BLOCK BY PARASPINOUS SAGITTAL SHIFT APPROACH |
- sensory and motor block level [ Time Frame: immediately after the intervention/procedure/surgery ]BY PIN PRICK
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| Ages Eligible for Study: | 30 Years to 60 Years (Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
-ASA I and II
Exclusion Criteria:
- Contraindications for regional blocks (eg. Patient refusal Infection at the injection site, coagulopathy)
- Allergic reaction to drugs.
- opium addiction, any drug or substance abuse and chronic treatment with opium, non-steroidal anti-inflammatory drugs
| Responsible Party: | doaa rashwan, Assistant professor Doaa Rashwan, Beni-Suef University |
| ClinicalTrials.gov Identifier: | NCT04628923 |
| Other Study ID Numbers: |
FMBSUREC/05072020/AbdEl Badei2 |
| First Posted: | November 16, 2020 Key Record Dates |
| Last Update Posted: | November 16, 2020 |
| Last Verified: | November 2020 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |

