Sun 2008.
Methods | Two‐arm, single‐centre, parallel‐group RCT, with 12 months of follow‐up |
Participants |
Location: China Setting of recruitment and treatment: Shenzhen People's Hospital Sample size:
Participant (baseline) characteristics:
Inclusion criteria: benign lesions of the parotid gland; aged over 18 years Exclusion criteria: not stated |
Interventions |
Intervention group (flap group): superficial parotidectomy + acellular dermal matrix Comparator group (no flap group): superficial parotidectomy Use of additional interventions: not stated |
Outcomes | Primary outcome: incidence rate of Frey's syndrome assessed clinically (Minor's starch‐iodine test) (assessed at 1 year after surgery); complications Secondary outcomes: incidence rate of Frey's syndrome assessed by participants (assessed at 1 year after surgery) |
Notes | We could not make contact with the authors to confirm whether randomisation was strictly performed |