Continuous Adductor Canal Block With a New Catheter - Primary Placement and Secondary Repositioning

Pain Clinical Trial

Official title:

Continuous Adductor Canal Block With a New Catheter - Primary Placement and Secondary Repositioning

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02657603
• Other study ID #: H-15016829
• Status: Completed
• Phase: N/A
• First received: January 11, 2016
• Last updated: October 18, 2017
• Start date: January 2016
• Est. completion date: March 2016

Study information

• Verified date: October 2017
• Source: Hillerod Hospital, Denmark
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a single center, randomized, blinded trial in healthy volunteers. The volunteers will receive bilateral placement of the new catheter corresponding to the adductor canal. Each volunteer will have a catheter placed in the adductor canal in both legs. The catheters are randomized to be placed either in the long-axis or short-axis plane of the adductor canal. Both catheters will be injected with local analgesics (LA). Allocation will be blinded to the volunteer and the investigator assessing sensory function. The volunteers will be sent home with the catheter in situ and return the following day. Injection with LA is repeated and sensory function is tested again. Furthermore catheter position is determined with ultrasound during injection. If sensory function is not affected by injection of LA then the catheter is visualized with ultrasound and repositioned followed by a second injection of LA and subsequent assessment of sensory function

Description:

3.2.1 Allocation concealment The volunteers are randomized using sealed opaque envelopes with a 1:1 ratio. The randomization defines which leg will be used for insertion of a catheter in the long-axis plane and which leg will be used for insertion in the short-axis plane of the adductor canal. The envelopes are prepared by health personnel with no relation to the study based on a computer-generated list.

3.2.2 Blinding Volunteers will be blinded to allocation. An opaque sterile draping will be used for insertion to prevent volunteers from observing the catheter insertion. After insertion the catheters will be covered with bandages to prevent unblinding of the volunteers. The investigator responsible for insertion of the catheters will leave the room after insertion and a separate assessor blinded to allocation will perform outcome assessments. On day 2 the investigator responsible for primary insertion will assess catheter position with ultra-sound (US), record a video for the assessors, injection of local anesthetics and cover the catheter in bandages. A separate blinded assessor will again perform the outcome assessment

3.2.3 Execution During catheter placement the volunteers are monitored using pulse oximetry and a secure intravenous access is obtained. A baseline sensory assessment is performed where cold sensation on the medial side of the lower leg is tested using alcohol swabs.

A peripheral nerve catheter will be inserted on each side under US guidance. This involves skin punctures at the site of insertion and at the exit site. To facilitate insertion the skin is locally infiltrated with lidocaine. Intravenous analgesia is provided if necessary (alfentanil 0.5mg/ml).

One catheter is inserted in the short-axis plane of the adductor canal using an in plane technique. The second catheter is inserted in the long-axis plane using a dynamic combination of in plane and out of plane techniques. 10ml of normal saline is used for hydro dissection in both catheters. When the catheters are in place 15 mL of LA (lidocaine 10mg/ml) is injected in each catheter. Distance from catheter orifice to artery is noted in the short axis group and distance from catheter orifice to fascia penetration is noted in the long axis group. After injection, the catheters are fixated to the skin with dressings.

Successful primary placement of the catheters will be tested 30 minutes after injection by a blinded investigator using a bilateral assessment of sensory function as described previously. Furthermore, cutaneous mapping is performed to assess affected cutaneous area.

Subsequently the volunteers are sent home with the catheter in situ and return the following day. The volunteers are instructed not to exercise -i.e. running, cycling, weight training etc.

On day 2 the catheter position is assessed with US during injection of LA and the distance from catheter orifice to artery/fascia is determined. A sensory assessment is performed. If there is no loss of cold sensation the catheter is registered as displaced and is therefore manually repositioned and injected with LA using US guidance. Assessment of cold sensation is repeated. Further, two investigators will independently watch a video clip of the injection procedure to assess whether the position is within the adductor canal. Total duration of participation for the individual volunteers will be 2 days.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 16
• Est. completion date: March 2016
• Est. primary completion date: March 2016
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Male or female =18 years of age.

• ASA classification = II. (ASA physical status classification system)

• Written informed consent obtained from subject and ability for subject to comply with the requirements of the study.

Exclusion Criteria:

• Distance from skin to adductor canal above 4 cm

• Previous or ongoing surgery, pain or other disability of the investigated region resulting in sensory or neurologic deficits in the investigated region.

• Allergy to LA.

• Pregnancy (all female participants will be tested for urine hCG), breastfeeding, or unwilling to practice birth control during participation in the study.

Related Conditions & MeSH terms

• Pain

Intervention

Drug:
• Lidocaine
Lidocaine injected through the new Catheter (LAX)
• Lidocaine
Lidocaine injected through the new Catheter (SAX)

Procedure:
• LAX insertion of catheter
ultra sound guided cather insertion in the long axis (LAX) of the adductor canal
• SAX insertion of catheter
ultra sound guided cather insertion in the short axis (SAX) of the adductor canal

Locations

Country	Name	City	State
Denmark	Nordsjællands Hospital	Hillerød

Sponsors (1)

Lead Sponsor	Collaborator
Kai Henrik Wiborg Lange

Country where clinical trial is conducted

Denmark, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Procedure time	time used from penetration of skin to needle exit.	1 hour
Other	insertion attempts	number of skin punctures for insertion	1 hour
Other	Affected skin area	cutaneous mapping of the skin area on the medial part of the lower with loss of cold sensation evaluated by application of an ice roller and outlining with a marker (pen) for comparison	1 hour
Primary	Loss of cold sensation	Loss of cold sensation after injection of Lidocaine(LA)	30 minutes after injection
Secondary	Discomfort during day 1	Rating on a scale from 1-10 overall, at rest and during activities and disturbance of sleep	1 day
Secondary	Loss of cold sensation on day 2 - indicating correct position of the catheter on day 2	loss of cold sensation on the medial part of the lower leg after LA injection on day 2	1 day after insertion
Secondary	Interrater agreement between 2 assessors whether catheter is within the adductor canal assessed by US video.	cohen's kappa for interrater agreement between assessments	1 day
Secondary	Displacement distance	Distance from catheter orifice to artery is noted in the short axis group and distance from catheter orifice to fascia penetration is noted in the long axis group	1 day
Secondary	Loss of cold sensation after repositioning if found to be displaced - Indicating successful repositioning	loss of cold sensation on the medial part of the lower leg after LA injection after attempted repositioning	1 day

External Links

•   cadaver study of the device