Clinical trial · Interventional
Effects of PECS 1 Block on Venous Cancer Port Catheter
Effects of Ultrasound Guided Pectoral Blok Type 1 on Subcutaneous Port Catheter Replacement : A Randomized Controlled Study
NCT04170699CI-TRIAL-00049892completedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
In this study our aim is to investigate the effects of ultrasound (USG) guided pectoral block (PECS) type 1 in the administration of an implanted port-a-cath .
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Catheter; Pain (Indwelling Catheter) | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Port-a-cath replacement | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- PECS 1 Block
- description
- 40 patients who had PECS 1 block for peroperative analgesia in port-a-cath replacement. All patients will receive IV Midazolam (0.05mg/kg) premedication. Standard monitorization of EKG, non- invasive blood pressure and pulseoximeter will be done and recorded in every 5 minutes. After sedation and standard monitorization, 20 minutes before the intervention and in the supine positon the PECS 1 block will be done. 10 % povidone - iodin will be used for sterilization and the USG probe will be covered with sterile sheath. The block will be done as a single injection of local anaesthetic between pectoralis major and pectoralis minor muscles at the level of the 3rd rib to anaesthetise the lateral and medial pectoral nerves. The USG probe will be replaced inferior to the clavicle. Identify the pectoralis muscles with the axillary artery and axillary vein on sonography. The brachial plexus should be visible underneath. After confirmation with 20 mL %0.25 bupivacaine will be administered.
- interventionNames
- Procedure: Port-a-cath replacement
- type
- EXPERIMENTAL
- label
- Infiltrative Anesthesia
- description
- 40 patients who had port-cath replacement will receive infiltrative anesthesia.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: * Ages between 18- 75 * ASA (American Society of Anesthesiologists) Score I-IV * Undergoing elective port-a-cath replacemnet Exclusion Criteria: * Patients with neurological deficits * Patients who have major vascular damage at the same side * Mentally retarded patients * Patients with alcohol or drug addiction * Patients who are allergic to local anesthetics * Pregnancy * Paitents with coagulopathy * Patients with skin infection at the side of the procedure * Patients with pneumothorax at the side of the procedure * Patient with a pacemaker
References
Publications (0)
Data not yet available
No reference posted for this study.