Adductor Canal Block Versus Femoral Nerve Block for Analgesia After Anterior Cruciate Ligament Reconstruction Arthroscopically
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| ClinicalTrials.gov Identifier: NCT02355093 |
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Recruitment Status : Unknown
Verified January 2015 by Daqiang Zhao, Shanghai Jiao Tong University Affiliated Sixth People's Hospital.
Recruitment status was: Enrolling by invitation
First Posted : February 4, 2015
Last Update Posted : February 4, 2015
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Anesthesia; Reaction | Procedure: adductor canal block (ACB) Procedure: Femoral nerve block (FNB) Drug: ropivacaine | Phase 4 |
| Study Type : | Interventional (Clinical Trial) |
| Estimated Enrollment : | 40 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Single (Participant) |
| Primary Purpose: | Treatment |
| Official Title: | Adductor Canal Block Versus Femoral Nerve Block for Analgesia After Anterior Cruciate Ligament Reconstruction Arthroscopically |
| Study Start Date : | July 2014 |
| Estimated Primary Completion Date : | March 2015 |
| Estimated Study Completion Date : | October 2015 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: adductor canal block (ACB)
We performed an ultrasound survey at the medial part of the thigh,the needle is introduced in-plane and 2 to 3 mL of saline is used to ensure correct placement of the needle in the vicinity of the saphenous nerve in the adductor canal,the catheter is introduced and advanced 1 to 2 cm beyond the tip of the needle.The study medication is administered as an infusion of 0.2% ropivacaine at a rate of 5mL/h during the next 48 hours.
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Procedure: adductor canal block (ACB)
We performed an ultrasound survey at the medial part of the thigh,the needle is introduced in-plane and 2 to 3 mL of saline is used to ensure correct placement of the needle in the vicinity of the saphenous nerve in the adductor canal,the catheter is introduced and advanced 1 to 2 cm beyond the tip of the needle.The study medication is administered as an infusion of 0.2% ropivacaine at a rate of 5mL/h during the next 48 hours. Drug: ropivacaine |
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Active Comparator: Femoral nerve block (FNB)
the catheter is inserted in-plane with the probe parallel to the inguinal crease, to obtain a short-axis view of the nerve. The correct needle placement is confirmed by injecting 2 to 3 mL of saline to cause tissue expansion below the iliac fascia, lateral to the femoral artery, and in the vicinity of the femoral nerve. The catheter is introduced 1 to 2 cm beyond the tip of the needle,an infusion of 0.2% ropivacaine at a rate of 5mL/h is administered during the next 48 hours.
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Procedure: Femoral nerve block (FNB)
the catheter is inserted in-plane with the probe parallel to the inguinal crease, to obtain a short-axis view of the nerve. The correct needle placement is confirmed by injecting 2 to 3 mL of saline to cause tissue expansion below the iliac fascia, lateral to the femoral artery, and in the vicinity of the femoral nerve. The catheter is introduced 1 to 2 cm beyond the tip of the needle,an infusion of 0.2% ropivacaine at a rate of 5mL/h is administered during the next 48 hours. Drug: ropivacaine |
- quadriceps muscle strength, as measured by handheld dynamometer. [ Time Frame: 3 days ]
- pain at rest time and during flexion of the knee, as measured by visual analog score(VAS). [ Time Frame: 3 days ]
- Dose of opioids [ Time Frame: 3 days ]
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| Ages Eligible for Study: | Child, Adult, Older Adult |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- ASA Ⅰ-Ⅲ
- Anterior Cruciate Ligament Reconstruction
Exclusion Criteria:
- patient refusal
- chronic use of opioids
- coagulation disorders
- infection at the puncture site
- allergic to anaesthetic
- preexisting neurological disorders
- communication difficulties
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02355093
| Principal Investigator: | Daqiang Zhao, Master | Shanghai Jiaotong University Affiliated Sixth People's Hospital Shanghai,China |
| Responsible Party: | Daqiang Zhao, Shanghai Jiao Tong University Affiliated Sixth People's Hospital |
| ClinicalTrials.gov Identifier: | NCT02355093 |
| Other Study ID Numbers: |
ACB vs FNB |
| First Posted: | February 4, 2015 Key Record Dates |
| Last Update Posted: | February 4, 2015 |
| Last Verified: | January 2015 |
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Ropivacaine Anesthetics, Local Anesthetics Central Nervous System Depressants |
Physiological Effects of Drugs Sensory System Agents Peripheral Nervous System Agents |

