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Evaluation of needle visibility during insertion of ultrasound guided transversus abdominis plane (TAP) blocks for women undergoing lower abdominal surgery.

In women receiving ultrasound guided transversus abdominis plane blocks for gynaecological or obstetric surgery is there a difference in the needle tip visibility when an echogenic needle is used compared to a non-echogenic needle.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12612000549820
Acronym
The SEETAP Trial
Enrollment
21
Registered
2012-05-23
Start date
2012-05-21
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

This trial is investigating whether echogenic needle technology improves needle visibility and ease of insertion when transversus abdominus plane (TAP) blocks are used for gynaecological and obstetric operations.

Interventions

All groups will undergo surgery under general anaesthesia. The anaesthetic technique will not be stipulated. At the end of surgery, whilst the patient is still asleep, bilateral TAP blocks will be inserted by the anaesthetist in theatre. Using an echogenic needle for one side and a non-echogenic needle for the other side. Real-time ultrasound guidance will be used to site the needle tip below the fascia with the TAP. Which needle is used first will be determined by the randomisation process. The

All groups will undergo surgery under general anaesthesia. The anaesthetic technique will not be stipulated. At the end of surgery, whilst the patient is still asleep, bilateral TAP blocks will be inserted by the anaesthetist in theatre. Using an echogenic needle for one side and a non-echogenic needle for the other side. Real-time ultrasound guidance will be used to site the needle tip below the fascia with the TAP. Which needle is used first will be determined by the randomisation process. The time taken to perform the TAP block on each side will be recorded from the time the needle goes through the skin until the time the injection of local anaesthetic is complete. The dose of local anaesthetic used will be 1.5mg/kg of ropivacaine diluted to a total volume of 20ml used each side. The maximal total dose will be 200mg ropivacaine. A 60 sec retrospective video clip of the ultrasound image will be recorded once 10mls of local anaesthetic has been injected.

Sponsors

King Edward Memorial Hospital for Women.
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

ASA 1 to 3 Elective or Non-elective abdominal gynaecological or obstetric surgery for which a TAP block will be used.

Exclusion criteria

Refusal or withdrawal of consent at any stage Anaphylaxis or hypersensitivity to local anaesthetics Non-English speaking

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026