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Awake Thoracic Epidural Anaesthesia Versus General Anesthesia for Video Assisted Thoracoscopic Surgery

A

Assiut University

Status and phase

Unknown
Phase 1

Conditions

Lung Cancer

Treatments

Procedure: Thoracic epidural anaesthesia video assisted thoracoscopic surgery

Study type

Interventional

Funder types

Other

Identifiers

NCT03902470
Anesthesia for VATS

Details and patient eligibility

About

Thoracic procedures are routinely performed under general anesthesia (GA), with one lung ventilation (OLV)by double lumen tube or (GA) in spontaneously breathing patient by TIVA or LMA are usually combined with thoracic epidural analgesia.

However, GA whether mechanically ventilated or spontaneously breathing may have adverse effects including peri-intubation hypoxia, trauma to the upper airway, mechanical ventilation-induced injuries, impaired cardiac performance, neuromuscular problems in OLV and increased risk of pneumonia, and release of proinflammatory mediators in generally.

Recently, awake thoracic epidural anesthesia (ATEA) has been used alone in thoracic procedures The results achieved in early studies have been encouraging. ATEA may eventually provide an alternative method to GA for thoracic procedures that would not only eliminate the need for GA but also facilitate both surgical reconstruction and eventually patient recovery.

Recent studies suggested better clinical outcomes with ATEA, including less intraoperative bleeding, a better control of postoperative pain, early mobilization and short hospital stay, oral intake tolerance, reduction of surgical stress response, reduction of intraoperative cardiac events, improvement of myocardial flow determinants and left ventricular function, and a reduction of complications including pulmonary, thrombotic and infectious events.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age range between 18 and 60 years.
  • ASA score equal to or less than III.
  • The absence of severe emphysema or clinical signs of active infectious disease.
  • The procedure is predicted to be completed within two hours.

Exclusion criteria

  • Patients with expected difficult airway management
  • Haemodynamically unstable patients
  • Obesity (body mass index >30)
  • Inexperienced and poorly cooperative surgical team
  • Coagulopathy (international normalized ratio >1.5)
  • Persistent cough or high airway secretion
  • Neurological disorders: risk of seizure, unable to cooperate, intracranial mass or brain oedema
  • Extensive pleural adhesions or previous pulmonary resections
  • Hypoxaemia (PaO2 <60) or hypercarbia (PCO2 >50)
  • Any contraindications for use of regional anesthesia technique

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

Thoracic epidural anaesthesia for vats
Experimental group
Description:
Patients in thoracic epidural (TE) group will pre-medicated using midazolam 3-4 mg intravenous (IV)and fentanyl 50 mcg intravenously(i.v.). Then patients will placed in the lateral decubitus position. An epidural catheter will be inserted between T3-T4 and T4-T5 for all thoracic procedures except sympathectomy and thymectomy. A test dose (5 ml) of 2% lidocaine will be given, followed by 15-20 ml of bupivacain 0.5% and 50 mcg of fentanyl. The objective is to achieve sensory and motor block between C7 and T7 levels. At this level diaphragmatic respiration is maintained. The anaesthesia level will be monitored by warm-cold discrimination.
Treatment:
Procedure: Thoracic epidural anaesthesia video assisted thoracoscopic surgery
General anesthesia for vats
Active Comparator group
Description:
Patients will receive general anesthesia as follows, Premedication in the form of 3-4 mg midazolam (IV), induction of a anesthesia with propofol (2mg/kg) and fentanyl (1 mcg/kg). Tracheal intubation and double endotracheal tube insertion will be facilitated with cisatracurium 0.1 mg/kg. and confirmation of it is position will made by fiberoptic bronchoscopy, Anesthesia will be maintained with isoflurane (1-2 %) and cisatracurium (0.05 mg/kg per dose).After the end of the operation, anesthesia will be discontinued, the wound dressing will be applied, and extubation of the patient will be done after reversal of muscle relaxant by neostigmine (0.05 mg/kg) and atropine (0.02 mg/kg) and extubation will be performed after complete neuromuscular recovery.
Treatment:
Procedure: Thoracic epidural anaesthesia video assisted thoracoscopic surgery

Trial contacts and locations

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Central trial contact

Mohamed Rabeea Ahmed

Data sourced from clinicaltrials.gov

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